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    I

    112TH CONGRESS1ST SESSION H. R. 1254

    To amend the Controlled Substances Act to place synthetic drugs in Schedule

    I.

    IN THE HOUSE OF REPRESENTATIVES

    MARCH 30, 2011

    Mr. DENT (for himself, Mr. MEEHAN, Mr. MARINO, Mr. PLATTS, Mr.BARLETTA, Mr. CUELLAR, Mrs. EMERSON, Mrs. BIGGERT, Mr.

    LATOURETTE, Mr. GIBSON, Mr. STIVERS, and Mr. REED) introduced the

    following bill; which was referred to the Committee on Energy and Com-

    merce, and in addition to the Committee on the Judiciary, for a period

    to be subsequently determined by the Speaker, in each case for consider-

    ation of such provisions as fall within the jurisdiction of the committee

    concerned

    A BILL

    To amend the Controlled Substances Act to place synthetic

    drugs in Schedule I.

    Be it enacted by the Senate and House of Representa-1

    tives of the United States of America in Congress assembled,2

    SECTION 1. SHORT TITLE.3

    This Act may be cited as the Synthetic Drug Con-4

    trol Act of 2011.5

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    HR 1254 IH

    SEC. 2. ADDITION OF SYNTHETIC DRUGS TO SCHEDULE I1

    OF THE CONTROLLED SUBSTANCES ACT.2

    (a) CANNABIMIMETIC AGENTS.Schedule I, as set3

    forth in section 202(c) of the Controlled Substances Act4

    (21 U.S.C. 812(c)) is amended by adding at the end the5

    following:6

    (d)(1) Unless specifically exempted or unless listed7

    in another schedule, any material, compound, mixture, or8

    preparation which contains any quantity of9

    cannabimimetic agents, or which contains their salts, iso-10

    mers, and salts of isomers whenever the existence of such11

    salts, isomers, and salts of isomers is possible within the12

    specific chemical designation.13

    (2) In paragraph (1), the term cannabimimetic14

    agents15

    (A) means any substance that is a cannabinoid16

    receptor type 1 (CB1 receptor) agonist as dem-17

    onstrated by binding studies and functional assays18

    within the following structural classes:19

    (i) 2-(3-hydroxycyclohexyl)phenol with20

    substitution at the 5-position of the phenolic21

    ring by alkyl or alkenyl, whether or not sub-22

    stituted on the cyclohexyl ring to any extent.23

    (ii) 3-(1-naphthoyl)indole or 3-(1-24

    naphthyl)indole by substitution at the nitrogen25

    atom of the indole ring, whether or not further26

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    HR 1254 IH

    substituted on the indole ring to any extent,1

    whether or not substituted on the naphthoyl or2

    naphthyl ring to any extent.3

    (iii) 3-(1-naphthoyl)pyrrole by substi-4

    tution at the nitrogen atom of the pyrrole ring,5

    whether or not further substituted in the indole6

    ring to any extent, whether or not substituted7

    on the naphthoyl ring to any extent.8

    (iv) 1-(1-naphthylmethyl)indene by substi-9

    tution of the 3-position of the indene ring,10

    whether or not further substituted in the indene11

    ring to any extent, whether or not substituted12

    on the naphthyl ring to any extent.13

    (v) 3-phenylacetylindole or 3-14

    benzoylindole by substitution at the nitrogen15

    atom of the indole ring, whether or not further16

    substituted in the indole ring to any extent,17

    whether or not substituted on the phenyl ring18

    to any extent.; and19

    (B) includes20

    (i) 5-(1,1-dimethylheptyl)-2-[(1R,3S)-3-21

    hydroxycyclohexyl]-phenol (CP-47,497);22

    (ii) 5-(1,1-dimethyloctyl)-2-[(1R,3S)-3-23

    hydroxycyclohexyl]-phenol (cannabicyclohexanol24

    or CP-47,497 C8-homolog);25

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    HR 1254 IH

    (iii) 1-pentyl-3-(1-naphthoyl)indole1

    (JWH-018 and AM678);2

    (iv) 1-butyl-3-(1-naphthoyl)indole (JWH-3

    073);4

    (v) 1-hexyl-3-(1-naphthoyl)indole (JWH-5

    019);6

    (vi) 1-[2-(4-morpholinyl)ethyl]-3-(1-naph-7

    thoyl)indole (JWH-200);8

    (vii) 1-pentyl-3-(2-9

    methoxyphenylacetyl)indole (JWH-250);10

    (viii) 1-pentyl-3-[1-(4-11

    methoxynaphthoyl)]indole (JWH-081);12

    (ix) 1-pentyl-3-(4-methyl-1-naph-13

    thoyl)indole (JWH-122);14

    (x) 1-pentyl-3-(4-chloro-1-naph-15

    thoyl)indole (JWH-398);16

    (xi) 1-(5-fluoropentyl)-3-(1-naph-17

    thoyl)indole (AM2201);18

    (xii) 1-(5-fluoropentyl)-3-(2-19

    iodobenzoyl)indole (AM694);20

    (xiii) 1-pentyl-3-[(4-methoxy)-ben-21

    zoyl]indole (SR-19 and RCS-4);22

    (xiv) 1-cyclohexylethyl-3-(2-23

    methoxyphenylacetyl)indole (SR-18 and RCS-24

    8); and25

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    HR 1254 IH

    (xv) 1-pentyl-3-(2-1

    chlorophenylacetyl)indole (JWH-203)..2

    (b) OTHER DRUGS.Schedule I of section 202(c) of3

    the Controlled Substances Act (21 U.S.C. 812(c)) is4

    amended in subsection (c) by adding at the end the fol-5

    lowing:6

    (18) 4-methylmethcathinone (Mephedrone).7

    (19) 3,4-methylenedioxypyrovalerone (MDPV).8

    (20) 3,4-methylenedioxymethcathinone9

    (methylone).10

    (21) Naphthylpyrovalerone (naphyrone).11

    (22) 4-fluoromethcathinone (flephedrone).12

    (23) 4-methoxymethcathinone (methedrone;13

    Bk-PMMA).14

    (24) Ethcathinone.15

    (25) 3,4-methylenedioxyethcathinone16

    (ethylone).17

    (26) Beta-keto-N-methyl-3,4-18

    benzodioxyolybutanamine (butylone).19

    (27) N,N-dimethylcathinone20

    (metamfepramone).21

    (28) Alpha-pyrrolidinopropiophenone (alpha-22

    PPP).23

    (29) 4-methoxy-alpha-24

    pyrrolidinopropiophenone (MOPPP).25

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    (30) 3,4-methylenedioxy-alpha-1

    pyrrolidinopropiophenone (MDPPP).2

    (31) Alpha-pyrrolidinovalerophenone (alpha-3

    PVP).4

    (32) 6,7-dihydro-5H-indeno(5,6-d)-1,3-dioxal-5

    6-amine) (MDAI)..6

    SEC. 3. TEMPORARY SCHEDULING TO AVOID IMMINENT7

    HAZARDS TO PUBLIC SAFETY EXPANSION.8

    Section 201(h)(2) of the Controlled Substances Act9

    (21 U.S.C. 811(h)(2)) is amended10

    (1) by striking one year and inserting 211

    years; and12

    (2) by striking six months and inserting 113

    year.14

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