【结 构 式】 |
【分子编号】61500 【品名】4-(benzyloxy)-3,5-dichlorobenzoic acid 【CA登记号】 |
【 分 子 式 】C14H10Cl2O3 【 分 子 量 】297.137 【元素组成】C 56.59% H 3.39% Cl 23.86% O 16.15% |
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:(I)Synthesis of the iodopropionic intermediate (IV) is achieved as follows. The condensation of 4-benzyloxy-3,5-dichlorobenzoic acid (I) with L-serine benzyl ester (II) by means of BOP and TEA in dichloromethane gives the benzoyl-serine (III), which is then converted into the target iodopropionic intermediate (IV) by reaction with MsCl and TEA, followed by treatment with NaI in acetone.
【1】 Watanabe, H.; Okue, M.; Kobayashi, H.; Kitahara, T.; The first synthesis of kaitocephalin based on the structure revision. Tetrahedron Lett 2002, 43, 5, 861. |
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) | 61500 | 4-(benzyloxy)-3,5-dichlorobenzoic acid | C14H10Cl2O3 | 详情 | 详情 | |
(II) | 38229 | benzyl (2S)-2-amino-3-hydroxypropanoate | C10H13NO3 | 详情 | 详情 | |
(III) | 61501 | benzyl (2S)-2-{[4-(benzyloxy)-3,5-dichlorobenzoyl]amino}-3-hydroxypropanoate | C24H21Cl2NO5 | 详情 | 详情 | |
(IV) | 61502 | benzyl (2R)-2-{[4-(benzyloxy)-3,5-dichlorobenzoyl]amino}-3-iodopropanoate | C24H20Cl2INO4 | 详情 | 详情 |
Extended Information