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【结 构 式】

【药物名称】Picenadol hydrochloride, LY-136595((-)-enantiomer), LY-136596((+)-enantiomer), LY-150720

【化学名称】(±)-trans-3-(1,3-Dimethyl-4-propyl-4-piperidinyl)phenol hydrochloride
      (±)-trans-m-(1,3-Dimethyl-4-propyl-4-piperidyl)phenol hydrochloride
      (±)-trans-1,3-Dimethyl-4-propyl-4-(3-hydroxyphenyl)piperidine hydrochloride

【CA登记号】74685-16-8, 79201-85-7 (free base)

【 分 子 式 】C16H26ClNO

【 分 子 量 】283.84472

【开发单位】Lilly (Originator)

【药理作用】ANALGESIC AND ANESTHETIC DRUGS, Analgesic Drugs, Opioid Analgesics, Opioid Agonists-Antagonists

合成路线1

The methylation of 2-methyl-3-propyl-3-(3-methoxyphenyl)-1-pyrroline (I) with dimethyl sulfate in refluxing butanone gives 1-methyl-3-propyl-2-exo-methylene-3-(3-methoxyphenyl)pyrrolidine (II), which by reaction with HBF4 in ethanol is converted into 1,2-dimethyl-3-propyl-3-(3-methoxyphenyl)pyrrolinium tetrafluoroborate (III). The methylation of (III) with diazomethane in dichloromethane ether yields 1,2-dimethyl-3-propyl-3-(3-methoxyphenyl)-1,2-ethylenepyrrolidinium tetrafluoroborate (IV), which by heating at 180 C and neutralization with NaOH affords 1,3-dimethyl-4-propyl-4-(3-methoxyphenyl)-1,4,5,6-tetrahydropyridine (V). The reduction of (V) with NaBH4 in THF gives 1,3-dimethyl-4-propyl-4-(3-methoxyphenyl)piperidine (VI), which is finally treated with 48% HBr in refluxing acetic acid.

1 Zimmerman, D.M. (Eli Lilly and Company); 1,3,4-Trisubstituted-4-arylpiperidines and their preparation. BE 0833044; DE 2539452; FR 2283679; FR 2299337; GB 1525584; JP 7648670; JP 7783572 .
2 Castaner, J.; Serradell, M.N.; Picedanol Hydrochloride. Drugs Fut 1984, 9, 3, 204.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 30363 4-(3-methoxyphenyl)-5-methyl-4-propyl-3,4-dihydro-2H-pyrrole; methyl 3-(5-methyl-4-propyl-3,4-dihydro-2H-pyrrol-4-yl)phenyl ether C15H21NO 详情 详情
(II) 30364 methyl 3-(1-methyl-2-methylene-3-propyl-3-pyrrolidinyl)phenyl ether; 3-(3-methoxyphenyl)-1-methyl-2-methylene-3-propylpyrrolidine C16H23NO 详情 详情
(III) 30365 4-(3-Methoxyphenyl)-1,5-dimethyl-4-propyl-3,4-dihydro-2H-pyrrolium tetraflluoroborate C16H24BF4NO 详情 详情
(IV) 30366 4-(3-Methoxyphenyl)-1,5-dimethyl-4-propyl-1-azoniabicyclo[3,1,0]hexane tetrafluoroborate C17H26BF4NO 详情 详情
(V) 30367 4-(3-methoxyphenyl)-1,5-dimethyl-4-propyl-1,2,3,4-tetrahydropyridine; 3-(1,5-dimethyl-4-propyl-1,2,3,4-tetrahydro-4-pyridinyl)phenyl methyl ether C17H25NO 详情 详情
(VI) 30368 (3S,4R)-4-(3-methoxyphenyl)-1,3-dimethyl-4-propylpiperidine; 3-[(3S,4R)-1,3-dimethyl-4-propylpiperidinyl]phenyl methyl ether C17H27NO 详情 详情
Extended Information