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【结 构 式】

【药物名称】Picumast dihydrochloride, BM-15100, Auteral

【化学名称】1-(4-Chlorobenzyl)-4-[3-(3,4-dimethylcoumarin-7-yloxy)propyl]piperazine dihydrochloride
      7-[3-[4-[(4-Chlorophenyl)methyl]-1-piperazinyl]propoxy]-3,4-dimethyl-2H-1-benzopyran-2-one dihydrochloride
      3,4-Dimethyl-7-[4-(4-chlorophenyl)methyl-1-piperazinyl]propoxycoumarin dihydrochloride

【CA登记号】39577-20-3, 39557-19-2 (free base)

【 分 子 式 】C25H31Cl3N2O3

【 分 子 量 】513.89642

【开发单位】Roche (Originator)

【药理作用】Antiallergy/Antiasthmatic Drugs, Asthma Therapy, RESPIRATORY DRUGS, Histamine H1 Antagonists, Mediator Release Inhibitors

合成路线1

The total synthesis of picumast dihydrochloride has been described: The alkylation of piperazine (I) with 4-chlorobenzyl chloride (II) in ethanol gives 1-(4-chlorobenzyl)piperazine (III), which is alkylated again with 1-bromo-3-chloropropane (IV) by means of triethylamine in a suitable solvent to yield 1-(4-chlorobenzyl)-4-(3-chloropropyl)piperazine (V). Finally, this compound is condensed with 7-hydroxy-3,4-dimethylcoumarin (VI) by means of K2CO3 in refluxing butanone. Compound (VI) is obtained by cyclization of resorcinol (VII) with ethyl 2-methylacetoacetate (VIII) by means of refluxing acetic acid containing HCl.

1 Witte, E.-C.; Chemical synthesis of picumast dihydrochloride. Arzneim-Forsch Drug Res 1989, 39, 10a, 1309.
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) 10355 Diethylenediamine; Piperazine 110-85-0 C4H10N2 详情 详情
(II) 10356 1-Chloro-4-(chloromethyl)benzene; 4-Chlorobenzyl chloride 104-83-6 C7H6Cl2 详情 详情
(III) 10357 1-(4-Chlorobenzyl)piperazine; N-(4-Chlorobenzyl)piperazine C11H15ClN2 详情 详情
(IV) 10358 1-Bromo-3-chloropropane 109-70-6 C3H6BrCl 详情 详情
(V) 10359 1-(4-Chlorobenzyl)-4-(3-chloropropyl)piperazine C14H20Cl2N2 详情 详情
(VI) 10360 3,4-Dimethylumbelliferone; 7-Hydroxy-3,4-dimethyl-2H-chromen-2-one 2107-78-0 C11H10O3 详情 详情
(VII) 10361 1,3-Dihydroxybenzene; m-Dihydroxybenzene; Resorcinol; Resorcin; 1,3-Benzenediol 108-46-3 C6H6O2 详情 详情
(VIII) 10362 ethyl 2-methyl-3-oxobutanoate; ethyl 2-methylacetoacetate 609-14-3 C7H12O3 详情 详情

合成路线2

By condensation of 7-hydroxy-3,4-dimethylcoumarin (I) with 1-(3-chloropropyl)-4-(4-chlorobenzyl)piperazine (II) by means of K2CO3 and KI in refluxing butanone.

1 Witte, E.C.; et al. (Boehringer Ingelheim GmbH); Coumarin-7-yloxyalkyl piperazine compounds. DE 2123924; FR 2137731; GB 1335946; JP 58219176; US 3810898 .
2 Hillier, K.; Castaner, J.; BM-15100. Drugs Fut 1977, 2, 7, 438.
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) 10359 1-(4-Chlorobenzyl)-4-(3-chloropropyl)piperazine C14H20Cl2N2 详情 详情
(II) 10360 3,4-Dimethylumbelliferone; 7-Hydroxy-3,4-dimethyl-2H-chromen-2-one 2107-78-0 C11H10O3 详情 详情
Extended Information