Misuse of Drugs (Miscellaneous
Amendments) (No. 3) (Jersey) Order 2013
Made 10th June 2013
Coming into force 17th
June 2013
THE MINISTER FOR HEALTH AND SOCIAL SERVICES, in pursuance of Articles 3(2)
and 27 of the Misuse of Drugs (Jersey) Law 1978[1], and on the recommendation of the
Advisory Council on the Misuse of Drugs, orders as follows –
1 Misuse of Drugs (Jersey) Law 1978
amended
(1) In paragraph 1
of Part 2 of Schedule 2 to the Misuse of Drugs (Jersey) Law 1978[2] –
(a) in
sub-paragraph (a) after the substance “Amphetamine” there
shall be inserted the substance “Buprenorphine”;
(b) in
sub-paragraph (a) after the substance “Dihydrocodeine” there
shall be inserted the substance –
“2-((Dimethylamino)methyl)-1-(3-hydroxyphenyl)cyclohexanol
(also known as O-desmethyltramadol)”;
(c) for
sub-paragraphs (c) to (g) of paragraph 1 there shall be substituted
the following sub-paragraphs –
“(c) the following substances –
[2,3-Dihydro-5-methyl-3-(4-morpholinylmethyl)pyrrolo[1,
2, 3-de]-1,4-benzoxazin-6-yl]-1-naphthalenylmethanone
3-Dimethylheptyl-11-hydroxyhexahydrocannabinol
[9-Hydroxy-6-methyl-3-[5-phenylpentan-2-yl]
oxy-5, 6, 6a, 7, 8, 9, 10, 10a-octahydrophenanthridin-1-yl] acetate
9-(Hydroxymethyl)-6,
6-dimethyl-3-(2-methyloctan-2-yl)-6a, 7, 10, 10a-tetrahydrobenzo[c]chromen-1-ol;
(d) any compound structurally derived from 3-(1-naphthoyl)indole,
3-(2-naphthoyl) indole, 1H-indol-3-yl-(1-naphthyl)methane or
1H-indol-3-yl-(2-naphthyl)methane by substitution at the nitrogen atom of the
indole ring by alkyl, haloalkyl, alkenyl, cyanoalkyl, hydroxyalkyl,
cycloalkylmethyl, cycloalkylethyl, (N-methylpiperidin-2-yl)methyl or 2-(4-morpholinyl)ethyl,
whether or not further substituted in the indole ring to any extent and whether
or not substituted in the naphthyl ring to any extent;
(e) any compound structurally derived from 3-(1-naphthoyl)pyrrole
or 3-(2-naphthoyl)pyrrole by substitution at the nitrogen atom of the pyrrole
ring by alkyl, haloalkyl, alkenyl, cyanoalkyl, hydroxyalkyl, cycloalkylmethyl,
cycloalkylethyl, (N-methylpiperidin-2-yl)methyl or 2-(4-morpholinyl)ethyl,
whether or not further substituted in the pyrrole ring to any extent and
whether or not substituted in the naphthyl ring to any extent;
(f) any compound structurally derived from
1-(1-naphthylmethylene)indene or 1-(2-naphthylmethylene)indene by substitution
at the 3-position of the indene ring by alkyl, haloalkyl, alkenyl, cyanoalkyl,
hydroxyalkyl, cycloalkylmethyl, cycloalkylethyl, (N-methylpiperidin-2-yl)methyl
or 2-(4-morpholinyl)ethyl, whether or not further substituted in the indene
ring to any extent and whether or not substituted in the naphthyl ring to any
extent;
(g) any compound structurally derived from 3-phenylacetylindole
by substitution at the nitrogen atom of the indole ring by alkyl, haloalkyl,
alkenyl, cyanoalkyl, hydroxyalkyl, cycloalkylmethyl, cycloalkylethyl, (N-methylpiperidin-2-yl)methyl
or 2-(4-morpholinyl)ethyl, whether or not further substituted in the indole
ring to any extent and whether or not substituted in the phenyl ring to any
extent;
(ga) any compound structurally derived from 2-(3-hydroxycyclohexyl)phenol
by substitution at the 5-position of the phenolic ring by alkyl, alkenyl,
cycloalkylmethyl, cycloalkylethyl or 2-(4-morpholinyl)ethyl, whether or not
further substituted in the cyclohexyl ring to any extent;
(gb) any compound structurally derived from
3-benzoylindole by substitution at the nitrogen atom of the indole ring by
alkyl, haloalkyl, alkenyl, cyanoalkyl, hydroxyalkyl, cycloalkylmethyl,
cycloalkylethyl, (N-methylpiperidin-2-yl)methyl or 2-(4-morpholinyl)ethyl,
whether or not further substituted in the indole ring to any extent and whether
or not substituted in the phenyl ring to any extent;
(gc) any compound structurally derived from
3-(1-adamantoyl)indole or 3-(2-adamantoyl)indole by substitution at the
nitrogen atom of the indole ring by alkyl, haloalkyl, alkenyl, cyanoalkyl,
hydroxyalkyl, cycloalkylmethyl, cycloalkylethyl, (N-methylpiperidin-2-yl)methyl
or 2-(4-morpholinyl)ethyl, whether or not further substituted in the indole
ring to any extent and whether or not substituted in the adamantyl ring to any
extent;
(gd) any compound structurally derived from
3-(2,2,3,3-tetramethylcyclopropylcarbonyl)indole by substitution at the
nitrogen atom of the indole ring by alkyl, haloalkyl, alkenyl, cyanoalkyl,
hydroxyalkyl, cycloalkylmethyl, cycloalkylethyl, (N-methylpiperidin-2-yl)methyl
or 2-(4-morpholinyl)ethyl, whether or not further substituted in the indole
ring to any extent;”;
(d) after
sub-paragraph (k) there shall be added the following sub-paragraph –
“(l) 1-Phenylcyclohexylamine
or any compound (not being ketamine, tiletamine or a compound for the time
being specified in paragraph 1(a) of Part 1 of this Schedule)
structurally derived from 1-Phenylcyclohexylamine or 2-Amino-2-phenylcyclohexanone
by modification in any of the following ways, that is to say –
(i) by
substitution at the nitrogen atom to any extent by alkyl, alkenyl or
hydroxyalkyl groups, or replacement of the amino group with a 1-piperidyl,
1-pyrrolidyl or 1-azepyl group, whether or not the nitrogen containing ring is
further substituted by one or more alkyl groups,
(ii) by
substitution in the phenyl ring to any extent by amino, alkyl, hydroxy, alkoxy
or halide substituents, whether or not further substituted in the phenyl ring to
any extent,
(iii) by
substitution in the cyclohexyl or cyclohexanone ring by one or more alkyl
substituents,
(iv) by
replacement of the phenyl ring with a thienyl ring.”.
(2) In
Part 3 of Schedule 2 to the Misuse of Drugs (Jersey) Law 1978 –
(a) in paragraph 1(a)
the substance “Buprenorphine” shall be deleted;
(b) paragraph 10
shall be deleted.
2 Misuse
of Drugs (General Provisions) (Jersey) Order 2009 amended
(1) In paragraph 1
of Schedule 1 to the Misuse of Drugs (General Provisions) (Jersey) Order 2009[3] –
(a) in
sub-paragraph (a) after the substance “2,5-Dimethoxy-a, 4-dimethylphenethylamine” there
shall be inserted the following substance –
“2-((Dimethylamino)methyl)-1-(3-hydroxyphenyl)cyclohexanol
(also known as O-desmethyltramadol)”;
(b) for
sub-paragraphs (l) to (p) there shall be substituted the following
sub-paragraphs –
“(l) the following
substances –
[2,3-Dihydro-5-methyl-3-(4-morpholinylmethyl)pyrrolo[1,
2, 3-de]-1,4-benzoxazin-6-yl]-1-naphthalenylmethanone
3-Dimethylheptyl-11-hydroxyhexahydrocannabinol
[9-Hydroxy-6-methyl-3-[5-phenylpentan-2-yl]
oxy-5, 6, 6a, 7, 8, 9, 10, 10a-octahydrophenanthridin-1-yl] acetate
9-(Hydroxymethyl)-6, 6-dimethyl-3-(2-methyloctan-2-yl)-6a,
7, 10, 10a-tetrahydrobenzo[c]chromen-1-ol;
(m) any compound structurally derived from 3-(1-naphthoyl)indole,
3-(2-naphthoyl) indole, 1H-indol-3-yl-(1-naphthyl)methane or
1H-indol-3-yl-(2-naphthyl)methane by substitution at the nitrogen atom of the
indole ring by alkyl, haloalkyl, alkenyl, cyanoalkyl, hydroxyalkyl,
cycloalkylmethyl, cycloalkylethyl, (N-methylpiperidin-2-yl)methyl or 2-(4-morpholinyl)ethyl,
whether or not further substituted in the indole ring to any extent and whether
or not substituted in the naphthyl ring to any extent;
(n) any compound structurally derived from 3-(1-naphthoyl)pyrrole
or 3-(2-naphthoyl)pyrrole by substitution at the nitrogen atom of the pyrrole
ring by alkyl, haloalkyl, alkenyl, cyanoalkyl, hydroxyalkyl, cycloalkylmethyl,
cycloalkylethyl, (N-methylpiperidin-2-yl)methyl or 2-(4-morpholinyl)ethyl,
whether or not further substituted in the pyrrole ring to any extent and
whether or not substituted in the naphthyl ring to any extent;
(o) any compound structurally derived from 1-(1-naphthylmethylene)indene
or 1-(2-naphthylmethylene)indene by substitution at the 3-position of the
indene ring by alkyl, haloalkyl, alkenyl, cyanoalkyl, hydroxyalkyl,
cycloalkylmethyl, cycloalkylethyl, (N-methylpiperidin-2-yl)methyl or 2-(4-morpholinyl)ethyl,
whether or not further substituted in the indene ring to any extent and whether
or not substituted in the naphthyl ring to any extent;
(p) any compound structurally derived from 3-phenylacetylindole
by substitution at the nitrogen atom of the indole ring by alkyl, haloalkyl, alkenyl,
cyanoalkyl, hydroxyalkyl, cycloalkylmethyl, cycloalkylethyl, (N-methylpiperidin-2-yl)methyl
or 2-(4-morpholinyl)ethyl, whether or not further substituted in the indole
ring to any extent and whether or not substituted in the phenyl ring to any extent;
(pa) any compound structurally derived from 2-(3-hydroxycyclohexyl)phenol
by substitution at the 5-position of the phenolic ring by alkyl, alkenyl,
cycloalkylmethyl, cycloalkylethyl or 2-(4-morpholinyl)ethyl, whether or not
further substituted in the cyclohexyl ring to any extent;
(pb) any compound structurally derived from
3-benzoylindole by substitution at the nitrogen atom of the indole ring by
alkyl, haloalkyl, alkenyl, cyanoalkyl, hydroxyalkyl, cycloalkylmethyl,
cycloalkylethyl, (N-methylpiperidin-2-yl)methyl or 2-(4-morpholinyl)ethyl,
whether or not further substituted in the indole ring to any extent and whether
or not substituted in the phenyl ring to any extent;
(pc) any compound structurally derived from
3-(1-adamantoyl)indole or 3-(2-adamantoyl)indole by substitution at the
nitrogen atom of the indole ring by alkyl, haloalkyl, alkenyl, cyanoalkyl,
hydroxyalkyl, cycloalkylmethyl, cycloalkylethyl, (N-methylpiperidin-2-yl)methyl
or 2-(4-morpholinyl)ethyl, whether or not further substituted in the indole
ring to any extent and whether or not substituted in the adamantyl ring to any
extent;
(pd) any compound structurally derived from
3-(2,2,3,3-tetramethylcyclopropylcarbonyl)indole by substitution at the
nitrogen atom of the indole ring by alkyl, haloalkyl, alkenyl, cyanoalkyl,
hydroxyalkyl, cycloalkylmethyl, cycloalkylethyl, (N-methylpiperidin-2-yl)methyl
or 2-(4-morpholinyl)ethyl, whether or not further substituted in the indole
ring to any extent;”;
(c) after
sub-paragraph (t) there shall be added the following sub-paragraph –
“(u) 1-phenylcyclohexylamine or
any compound (not being eticyclidine, ketamine, phencyclidine, rolicyclidine,
tenocyclidine or tiletamine) structurally derived from 1-phenylcyclohexylamine
or 2-amino-2-phenylcyclohexanone by modification in any of the following ways,
that is to say –
(i) by
substitution at the nitrogen atom to any extent by alkyl, alkenyl or
hydroxyalkyl groups, or replacement of the amino group with a 1-piperidyl,
1-pyrrolidyl or 1-azepyl group, whether or not the nitrogen containing ring is
further substituted by one or more alkyl groups,
(ii) by
substitution in the phenyl ring to any extent by amino, alkyl, hydroxy, alkoxy
or halide substituents, whether or not further substituted in the phenyl ring
to any extent,
(iii) by
substitution in the cyclohexyl or cyclohexanone ring by one or more alkyl
substituents,
(iv) by
replacement of the phenyl ring with a thienyl ring.”.
(2) For
paragraph 3 of Schedule 1 to the Misuse of Drugs (General Provisions)
(Jersey) Order 2009 there shall be substituted the following paragraphs –
“3. Any ester or ether of a
substance specified in paragraph 1 (not being
2-((dimethylamino)methyl)-1-(3-hydroxyphenyl)cyclohexanol).”.
“3A. Any ester or ether of a substance
specified in paragraph 2.”;
(3) Paragraph 6
of Schedule 1 to the Misuse of Drugs (General Provisions) (Jersey) Order 2009
shall be deleted.
3 Misuse
of Drugs (Designation) (Jersey) Order 1989 amended
In Part 1 of the Schedule to the Misuse of Drugs (Designation)
(Jersey) Order 1989[4] –
(a) in
sub-paragraph (a) of paragraph 1 after the substance “2,5-Dimethoxy-a,
4-dimethylphenethylamine” there shall be inserted the following substance –
“2-((Dimethylamino)methyl)-1-(3-hydroxyphenyl)cyclohexanol
(also known as O-desmethyltramadol)”;
(b) for
sub-paragraphs (j) to (n) of paragraph 1 there shall be substituted
the following sub-paragraphs –
“(j) the following
substances –
[2,3-Dihydro-5-methyl-3-(4-morpholinylmethyl)pyrrolo[1,
2, 3-de]-1,4-benzoxazin-6-yl]-1-naphthalenylmethanone
3-Dimethylheptyl-11-hydroxyhexahydrocannabinol
[9-Hydroxy-6-methyl-3-[5-phenylpentan-2-yl]
oxy-5, 6, 6a, 7, 8, 9, 10, 10a-octahydrophenanthridin-1-yl] acetate
9-(Hydroxymethyl)-6, 6-dimethyl-3-(2-methyloctan-2-yl)-6a,
7, 10, 10a-tetrahydrobenzo[c]chromen-1-ol;
(k) any compound structurally derived from 3-(1-naphthoyl)indole,
3-(2-naphthoyl) indole, 1H-indol-3-yl-(1-naphthyl)methane or
1H-indol-3-yl-(2-naphthyl)methane by substitution at the nitrogen atom of the
indole ring by alkyl, haloalkyl, alkenyl, cyanoalkyl, hydroxyalkyl,
cycloalkylmethyl, cycloalkylethyl, (N-methylpiperidin-2-yl)methyl or 2-(4-morpholinyl)ethyl,
whether or not further substituted in the indole ring to any extent and whether
or not substituted in the naphthyl ring to any extent;
(l) any compound structurally derived from
3-(1-naphthoyl)pyrrole or 3-(2-naphthoyl)pyrrole by substitution at the
nitrogen atom of the pyrrole ring by alkyl, haloalkyl, alkenyl, cyanoalkyl,
hydroxyalkyl, cycloalkylmethyl, cycloalkylethyl, (N-methylpiperidin-2-yl)methyl
or 2-(4-morpholinyl)ethyl, whether or not further substituted in the pyrrole
ring to any extent and whether or not substituted in the naphthyl ring to any
extent;
(m) any compound structurally derived from 1-(1-naphthylmethylene)indene
or 1-(2-naphthylmethylene)indene by substitution at the 3-position of the
indene ring by alkyl, haloalkyl, alkenyl, cyanoalkyl, hydroxyalkyl,
cycloalkylmethyl, cycloalkylethyl, (N-methylpiperidin-2-yl)methyl or 2-(4-morpholinyl)ethyl,
whether or not further substituted in the indene ring to any extent and whether
or not substituted in the naphthyl ring to any extent;
(n) any compound structurally derived from 3-phenylacetylindole
by substitution at the nitrogen atom of the indole ring by alkyl, haloalkyl,
alkenyl, cyanoalkyl, hydroxyalkyl, cycloalkylmethyl, cycloalkylethyl,
(N-methylpiperidin-2-yl)methyl or 2-(4-morpholinyl)ethyl, whether or not
further substituted in the indole ring to any extent and whether or not
substituted in the phenyl ring to any extent;
(na) any compound structurally derived from 2-(3-hydroxycyclohexyl)phenol
by substitution at the 5-position of the phenolic ring by alkyl, alkenyl,
cycloalkylmethyl, cycloalkylethyl or 2-(4-morpholinyl)ethyl, whether or not
further substituted in the cyclohexyl ring to any extent;
(nb) any compound structurally derived from
3-benzoylindole by substitution at the nitrogen atom of the indole ring by
alkyl, haloalkyl, alkenyl, cyanoalkyl, hydroxyalkyl, cycloalkylmethyl,
cycloalkylethyl, (N-methylpiperidin-2-yl)methyl or 2-(4-morpholinyl)ethyl,
whether or not further substituted in the indole ring to any extent and whether
or not substituted in the phenyl ring to any extent;
(nc) any compound structurally derived from
3-(1-adamantoyl)indole or 3-(2-adamantoyl)indole by substitution at the
nitrogen atom of the indole ring by alkyl, haloalkyl, alkenyl, cyanoalkyl,
hydroxyalkyl, cycloalkylmethyl, cycloalkylethyl, (N-methylpiperidin-2-yl)methyl
or 2-(4-morpholinyl)ethyl, whether or not further substituted in the indole
ring to any extent and whether or not substituted in the adamantyl ring to any
extent;
(nd) any compound structurally derived from
3-(2,2,3,3-tetramethylcyclopropylcarbonyl)indole by substitution at the
nitrogen atom of the indole ring by alkyl, haloalkyl, alkenyl, cyanoalkyl,
hydroxyalkyl, cycloalkylmethyl, cycloalkylethyl, (N-methylpiperidin-2-yl)methyl
or 2-(4-morpholinyl)ethyl, whether or not further substituted in the indole
ring to any extent;”;
(c) after
sub-paragraph (o) of paragraph 1 there shall be added the following
sub-paragraph –
“(p) 1-phenylcyclohexylamine or
any compound (not being eticyclidine, ketamine, phencyclidine, rolicyclidine,
tenocyclidine or tiletamine) structurally derived from 1-phenylcyclohexylamine
or 2-amino-2-phenylcyclohexanone by modification in any of the following ways,
that is to say –
(i) by
substitution at the nitrogen atom to any extent by alkyl, alkenyl or
hydroxyalkyl groups, or replacement of the amino group with a 1-piperidyl,
1-pyrrolidyl or 1-azepyl group, whether or not the nitrogen containing ring is
further substituted by one or more alkyl groups,
(ii) by
substitution in the phenyl ring to any extent by amino, alkyl, hydroxy, alkoxy
or halide substituents, whether or not further substituted in the phenyl ring
to any extent,
(iii) by
substitution in the cyclohexyl or cyclohexanone ring by one or more alkyl
substituents,
(iv) by
replacement of the phenyl ring with a thienyl ring.”;
(d) for
paragraph 3 there shall be substituted the following paragraphs –
“3. Any ester or ether of a
substance specified in paragraph 1 (not being
2-((dimethylamino)methyl)-1-(3-hydroxyphenyl)cyclohexanol).”.
“3A. Any ester or ether of a substance
specified in paragraph 2.”.
4 Citation
and commencement
This Order may be cited as the Misuse of Drugs (Miscellaneous
Amendments) (No. 3) (Jersey) Order 2013 and shall come into force
7 days after it is made.
deputy a.e. pryke of trinity
Minister for Health and Social Services