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【结 构 式】

【分子编号】18243

【品名】4-nitrobenzyl 7-[4-[((2S,4S)-4-(acetylsulfanyl)-1-[[(4-nitrobenzyl)oxy]carbonyl]pyrrolidinyl)carbonyl]-1-piperazinyl]-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-3-quinolinecarboxylate

【CA登记号】

【 分 子 式 】C39H37FN6O11S

【 分 子 量 】816.8210232

【元素组成】C 57.35% H 4.57% F 2.33% N 10.29% O 21.55% S 3.93%

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:(III)

Coupling of thioacetylproline derivative (I) with p-nitrobenzyl ester of ciprofloxacin (II) in the presence of dicyclohexylcarbodiimide (DCC) and 4-dimethylaminopyridine (DMAP) provided amide (III). Treatment with pyrrolidine in acetonitrile gave thiol (IV), which was subsequently alkylated with the carbapenem phosphate (V) in the presence of diisopropylethylamine to give thioether (VI). Then, hydrogenolytical removal of p-nitrobenzyl protecting groups in the presence of Pd-C, followed by treatment with sodium 2-ethylhexanoate in acetone provided the target disodium salt.

1 Hershberger, P.M.; Switzer, A.G.; Yelm, K.E.; Coleman, M.C.; Devries, C.A.; Rourke, F.J.; Davis, B.W.; Kraft, W.G.; Twinem, T.L.; Koenigs, P.M.; Paule, S.M.; Siehnel, R.J.; Zoutendam, P.H.; Imbus, R.; Demuth, T.P. Jr.; Preparation and antimicrobial assessment of 2-thioether-linked quinolonyl-carbapenems. J Antibiot 1998, 51, 9, 857-871.
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) 18241 (2S,4S)-4-(acetylsulfanyl)-1-[[(4-nitrobenzyl)oxy]carbonyl]-2-pyrrolidinecarboxylic acid C15H16N2O7S 详情 详情
(II) 18242 4-nitrobenzyl 1-cyclopropyl-6-fluoro-4-oxo-7-(1-piperazinyl)-1,4-dihydro-3-quinolinecarboxylate C24H23FN4O5 详情 详情
(III) 18243 4-nitrobenzyl 7-[4-[((2S,4S)-4-(acetylsulfanyl)-1-[[(4-nitrobenzyl)oxy]carbonyl]pyrrolidinyl)carbonyl]-1-piperazinyl]-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-3-quinolinecarboxylate C39H37FN6O11S 详情 详情
(IV) 18244 4-nitrobenzyl 1-cyclopropyl-6-fluoro-7-[4-[((2S,4S)-1-[[(4-nitrobenzyl)oxy]carbonyl]-4-sulfanylpyrrolidinyl)carbonyl]-1-piperazinyl]-4-oxo-1,4-dihydro-3-quinolinecarboxylate C37H35FN6O10S 详情 详情
(V) 13224 4-nitrobenzyl (4R,5R,6S)-3-[(diphenoxyphosphoryl)oxy]-6-[(1R)-1-hydroxyethyl]-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate 90776-59-3 C29H27N2O10P 详情 详情
(VI) 18246 4-nitrobenzyl 1-cyclopropyl-6-fluoro-7-[4-[((2S,4S)-4-[((4R,5S,6S)-6-[(1R)-1-hydroxyethyl]-4-methyl-2-[[(4-nitrobenzyl)oxy]carbonyl]-7-oxo-1-azabicyclo[3.2.0]hept-2-en-3-yl)sulfanyl]-1-[[(4-nitrobenzyl)oxy]carbonyl]pyrrolidinyl)carbonyl]-1-piperazinyl]-4-oxo-1,4-dihydro-3-quinolinecarboxylate C54H51FN8O16S 详情 详情
Extended Information