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【结 构 式】 
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【分子编号】41583 【品名】(2R)-2-[[(2S)-3-(benzoylsulfanyl)-2-methylpropanoyl]amino]-3-[[4-(dimethylamino)benzyl]sulfanyl]propionic acid 【CA登记号】 |
【 分 子 式 】C23H28N2O4S2 【 分 子 量 】460.6184 【元素组成】C 59.97% H 6.13% N 6.08% O 13.89% S 13.92% |
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：(IX)(S)-3-Benzoylthio-2-methylpropionic acid (VI) was activated as the acid chloride (VII) by treatment with SOCl2 or optionally converted to the active ester (VIII) upon condensation with p-nitrophenol in the presence of DCC. Coupling of aminoacid (V) with either acid chloride (VII) under Schotten-Baumann conditions or with p-nitrophenyl ester (VIII) in the presence of Et3N gave rise to the corresponding amide (IX). The benzoyl thioester of (IX) was finally cleaved employing aqueous ammonia to afford the title thiol.
| 【1】 Miyake, Y.; Horiuchi, M.; Mita, S.; Tsuji, F.; Involvement of leukotriene B4 in murine dermatitis models. Biochem Pharmacol 1998, 55, 297. |
| 【2】 Kawashima, Y.; Horiuchi, M. (Santen Pharmaceutical Co., Ltd.); Novel amino acid derivs. having N,N-dialkylaminophenyl group. EP 0870762; JP 1996301840; WO 9627585 . |
| 中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
|---|---|---|---|---|---|---|
| (V) | 41582 | (2R)-2-amino-3-[[4-(dimethylamino)benzyl]sulfanyl]propionic acid | C12H18N2O2S | 详情 | 详情 | |
| (VI) | 35379 | (2S)-3-(benzoylsulfanyl)-2-methylpropionic acid | C11H12O3S | 详情 | 详情 | |
| (VII) | 41584 | S-[(2R)-3-chloro-2-methyl-3-oxopropyl] benzenecarbothioate | C11H11ClO2S | 详情 | 详情 | |
| (VIII) | 35380 | 4-nitrophenyl (2S)-3-(benzoylsulfanyl)-2-methylpropanoate | C17H15NO5S | 详情 | 详情 | |
| (IX) | 41583 | (2R)-2-[[(2S)-3-(benzoylsulfanyl)-2-methylpropanoyl]amino]-3-[[4-(dimethylamino)benzyl]sulfanyl]propionic acid | C23H28N2O4S2 | 详情 | 详情 |
Extended Information