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【结 构 式】

【分子编号】48471

【品名】(6R,7R)-2-[(benzhydryloxy)carbonyl]-3-[[methyl(dimethylene)-lambda(6)-sulfanyl]oxy]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-7-aminium 4-methylbenzenesulfonate

【CA登记号】

【 分 子 式 】C30H32N2O7S3

【 分 子 量 】628.79136

【元素组成】C 57.31% H 5.13% N 4.46% O 17.81% S 15.3%

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:(XVII)

Alternatively, derivative (XV) can be obtained from the corresponding mesylate derivative: Treatment of alcohol (I) with MsCl and Et3N in CH2Cl2 yields methansulfonyl derivative (XVI), which is then converted into mesylated aminochlorocephalosporanic acid derivative (XVII) by following these steps: First treatment with metachloroperbenzoic acid (MCPBA) in dichloromethane, followed by reaction with KI and Tf2O in acetonitrile, chlorination with PCl5 and pyridine in dichloromethane, treatment with iBuOH and acidic treatment with TosOH. Condensation of derivative (XVII) with 7-chlorothiazole derivative (VII) by means of (PhO)2POCl in THF provides acetamido derivative (XVIII), which is then treated with chloropyridine derivative (XIV) and NaSH in DMF in DMF to afford compound (XV).

1 Glinka, T.W.; et al.; SAR studies of anti-MRSA non-zwitterionic 3-heteroarylthiocephems. J Antibiot 2000, 53, 10, 1045.
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) 37977 benzhydryl (6R,7R)-3-hydroxy-8-oxo-7-[(2-phenylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate C28H24N2O5S 详情 详情
(VII) 48463 2-(2-amino-5-chloro-1,3-thiazol-4-yl)-2-[(trityloxy)imino]acetic acid C24H18ClN3O3S 详情 详情
(XIV) 48468 tert-butyl 2-[[(4-chloro-2-pyridinyl)methyl]sulfanyl]ethylcarbamate C13H19ClN2O2S 详情 详情
(XV) 48469 benzhydryl (6R,7R)-7-([2-(2-amino-5-chloro-1,3-thiazol-4-yl)-2-[(trityloxy)imino]acetyl]amino)-3-([2-[([2-[(tert-butoxycarbonyl)amino]ethyl]sulfanyl)methyl]-4-pyridinyl]sulfanyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate C57H52ClN7O7S4 详情 详情
(XVI) 48470 benzhydryl (6R,7R)-3-[[methyl(dimethylene)-lambda(6)-sulfanyl]oxy]-8-oxo-7-[(2-phenylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate C31H30N2O5S2 详情 详情
(XVII) 48471 (6R,7R)-2-[(benzhydryloxy)carbonyl]-3-[[methyl(dimethylene)-lambda(6)-sulfanyl]oxy]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-7-aminium 4-methylbenzenesulfonate C30H32N2O7S3 详情 详情
(XVIII) 48472 benzhydryl (6R,7R)-7-([2-(2-amino-5-chloro-1,3-thiazol-4-yl)-2-[(trityloxy)imino]acetyl]amino)-3-[[methyl(dimethylene)-lambda(6)-sulfanyl]oxy]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate C47H40ClN5O6S3 详情 详情
Extended Information