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【结 构 式】

【药物名称】Gastrophenzine, DZO-200, AN5

【化学名称】4-(4-Chlorophenyl)-8-(ethoxycarbonylamino)-2-methyl-1,2,3,4-tetrahydroisoquinoline monohydrochloride
      [4-(4-Chlorophenyl)-2-methyl-1,2,3,4-tetrahydro-8-isoquinolinyl]carbamic acid ethyl ester monohydrochloride

【CA登记号】89845-17-0

【 分 子 式 】C19H22Cl2N2O2

【 分 子 量 】381.30539

【开发单位】Egis (Originator), Pharmachim (Originator)

【药理作用】Antidepressants, Antiulcer Drugs, Gastric Antisecretory Drugs, GASTROINTESTINAL DRUGS, Mood Disorders, Treatment of, PSYCHOPHARMACOLOGIC DRUGS

合成路线1

Two related methods have been described: The alkylation of 2-nitrobenzylmethylamine (I) with p-chlorphenyloxyran (II) in boiling ethanol affords N-(2-nitrobenzyl)-2-(methylamino)-1-(4-chlorphenyl)-1-ethanol (III), which is further reduced via NaBH4/NiCl2 in boiling methanol to N-(2-aminobenzyl)-2-(methylamino)-1-(4-chlorphenyl)-1-ethanol (IV). The acylation of (IV) with ethyl chloroformate in the presence of pyridine and in a medium of benzene - DMFA (Method A) results in N-[2-(ethoxycarbonyl)amino]-2-(methylamino)-1-(4-chlorophenyl)-1-ethanol (V). The latter is cyclodehydrated by means of conc.H2SO4 in dichloroethane. According to method B, the amino alcohol (IV) is cyclodehydrated by conc.H2SO4 to 8-amino-4-(4-chlorophenyl)-2-methyl-1,2,3-4-tetrahydroisoquinoline (VI), which is acylated with ethyl chloroformate in boiling benzene.

1 Ivanova, N.; Ivanov, T.; Mondeshka, D.; Berova, N.; Angelova, I.; Rakovska, R.; Bojadjiev, S.; Tancheva, C.; Tascheva, D.; Synthesis, stereochemistry, and antiulcer activity of 4-phenyltetrahydroisoquinolines. Arch Pharm 1990, 323, 1, 3.
2 Ivanova, N.; Angelova, J.; Mondeshka, D.; Ivanov, C.; Gastrophenzine. Drugs Fut 1992, 17, 2, 104.
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) 15242 N-methyl(2-nitrophenyl)methanamine; N-methyl-N-(2-nitrobenzyl)amine C8H10N2O2 详情 详情
(II) 15243 2-(4-chlorophenyl)oxirane C8H7ClO 详情 详情
(III) 15244 1-(4-chlorophenyl)-2-[methyl(2-nitrobenzyl)amino]-1-ethanol C16H17ClN2O3 详情 详情
(IV) 15245 2-[(2-aminobenzyl)(methyl)amino]-1-(4-chlorophenyl)-1-ethanol C16H19ClN2O 详情 详情
(V) 15246 ethyl N-(2-[[[2-(4-chlorophenyl)-2-hydroxyethyl](methyl)amino]methyl]phenyl)carbamate C19H23ClN2O3 详情 详情
(VI) 15247 4-(4-chlorophenyl)-2-methyl-1,2,3,4-tetrahydro-8-isoquinolinamine; 4-(4-chlorophenyl)-2-methyl-1,2,3,4-tetrahydro-8-isoquinolinylamine C16H17ClN2 详情 详情
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