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【结 构 式】

【分子编号】30232

【品名】4-bromo-2-methylphenyl isothiocyanate; 4-bromo-1-isothiocyanato-2-methylbenzene

【CA登记号】19241-38-4

【 分 子 式 】C8H6BrNS

【 分 子 量 】228.11238

【元素组成】C 42.12% H 2.65% Br 35.03% N 6.14% S 14.06%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(X)

In a further procedure, the bromophenyl imidazole (XIII) was prepared by treatment of 4-bromo-2-methylaniline (IX) with carbon disulfide and DCC to produce isothiocyanate (X). Condensation with 2,2-diethoxyethylamine (XI) gave thiourea (XII), which was cyclized in refluxing 8 N HCl to the 1-aryl-2-mercaptoimidazole (XIII). This was alkylated with the chloropropoxy quinolinone (XIV) to give sulfide (XV). Sharpless oxidation in the presence of D-diethyl tartrate produced the (S)-sulfoxide (XVI). Finally, hydrogenolysis of the halogen atom over Pd/C furnished the title compound.

1 Nishi, T.; Uno, T.; Shu, Y.; Tamura, K.; Okada, M. (Otsuka Pharmaceutical Co., Ltd.); Carbostyril derivs.. EP 0651747; JP 1995033765; US 5541198; WO 9426732 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(IX) 30231 4-bromo-2-methylphenylamine; 4-bromo-2-methylaniline 583-75-5 C7H8BrN 详情 详情
(X) 30232 4-bromo-2-methylphenyl isothiocyanate; 4-bromo-1-isothiocyanato-2-methylbenzene 19241-38-4 C8H6BrNS 详情 详情
(XI) 30233 3,3-diethoxypropylamine; 3,3-diethoxy-1-propanamine 41365-75-7 C7H17NO2 详情 详情
(XII) 30234 N-(4-bromo-2-methylphenyl)-N'-(3,3-diethoxypropyl)thiourea C15H23BrN2O2S 详情 详情
(XIII) 30235 1-(4-bromo-2-methylphenyl)-1H-imidazol-2-ylhydrosulfide; 1-(4-bromo-2-methylphenyl)-1H-imidazole-2-thiol C10H9BrN2S 详情 详情
(XIV) 30236 6-(3-chloropropoxy)-3,4-dihydro-2(1H)-quinolinone C12H14ClNO2 详情 详情
(XV) 30237 6-(3-[[1-(4-bromo-2-methylphenyl)-1H-imidazol-2-yl]sulfanyl]propoxy)-3,4-dihydro-2(1H)-quinolinone C22H22BrN3O2S 详情 详情
(XVI) 30238 6-(3-[[1-(4-bromo-2-methylphenyl)-1H-imidazol-2-yl]sulfinyl]propoxy)-3,4-dihydro-2(1H)-quinolinone C22H22BrN3O3S 详情 详情
Extended Information