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【结 构 式】

【药物名称】DPJ-489

【化学名称】1-[(3beta,16beta,17beta)-17-(Acetoxy)-3-(1-methylpyrrolidinio)androst-5-en-16-yl]-1-methylpiperidinium diiodide
      (3beta,16beta,17beta)-17-(Acetoxy)-16-(1-methylpiperidinium-1-yl)-3-(1-methyl-1-pyrrolidiniumyl)androst-5-ene diiodide

【CA登记号】350026-81-2

【 分 子 式 】C32H54I2N2O2

【 分 子 量 】752.60818

【开发单位】Panjab University (Originator), University of Strathclyde (Originator)

【药理作用】Adjuncts to Anesthesia, ANALGESIC AND ANESTHETIC DRUGS, Neuromuscular Blockers, Non-depolarizing Blocking Drugs

合成路线1

Condensation of 16-alpha-bromo-3-beta-hydroxy-5-androsten-17-one (I) with piperidine (II) produced the 16-piperidino derivative (III). Oppenauer oxidation of alcohol (III) with concomitant double-bond migration afforded the unsaturated ketone (IV), which was subsequently condensed with pyrrolidine (V) to yield the dienamine (VI). Reduction of the enamine and ketone functions of (VI) with NaBH4 gave the pyrrolidino alcohol (VII). This was then esterified with acetic anhydride in hot pyridine, yielding acetate (VIII). Finally, quaternization of (VIII) with methyl iodide provided the title bis-ammonium salt.

1 Fajrak, H.; Piplani, P.; Marshall, I.G.; Prior, C.; Jindal, D.P.; Synthesis and neuromuscular blocking activity of 16beta-piperidinosteroidal derivatives. Eur J Med Chem 2001, 36, 2, 195.
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) 30080 (3S,8R,9S,10R,13S,14S,16R)-16-bromo-3-hydroxy-10,13-dimethyl-1,2,3,4,7,8,9,10,11,12,13,14,15,16-tetradecahydro-17H-cyclopenta[a]phenanthren-17-one C19H27BrO2 详情 详情
(II) 10158 Piperidine 110-89-4 C5H11N 详情 详情
(III) 50970 (3S,8R,9S,10R,13S,14S,16S)-3-hydroxy-10,13-dimethyl-16-(1-piperidinyl)-1,2,3,4,7,8,9,10,11,12,13,14,15,16-tetradecahydro-17H-cyclopenta[a]phenanthren-17-one C24H37NO2 详情 详情
(IV) 50971 (8R,9S,10R,13S,14S,16S)-10,13-dimethyl-16-(1-piperidinyl)-3-(1-pyrrolidinyl)-1,2,7,8,9,10,11,12,13,14,15,16-dodecahydro-17H-cyclopenta[a]phenanthren-17-one C28H42N2O 详情 详情
(V) 11376 Pyrrolidine 123-75-1 C4H9N 详情 详情
(VI) 50972 (3S,8R,9S,10R,13S,14S,16S,17R)-10,13-dimethyl-16-(1-piperidinyl)-3-(1-pyrrolidinyl)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-ol C28H46N2O 详情 详情
(VII) 50973 (3S,8R,9S,10R,13S,14S,16S,17R)-10,13-dimethyl-16-(1-piperidinyl)-3-(1-pyrrolidinyl)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl acetate C30H48N2O2 详情 详情
(VIII) 50974 (1S,2S,13R,21R)-14-oxa-11,22-diazaheptacyclo[13.9.1.0(1,13).0(2,21).0(4,12).0(5,10).0(19,25)]pentacosa-4(12),5,7,9,15(25),16,18-heptaene-2,16-diol C22H20N2O3 详情 详情
Extended Information