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【结 构 式】

【分子编号】59315

【品名】 

【CA登记号】

【 分 子 式 】C35H44B4I6K4N6O23

【 分 子 量 】1877.82502

【元素组成】C 22.39% H 2.36% B 2.3% I 40.55% K 8.33% N 4.48% O 19.6%

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:(IV)

In a different strategy, the acetamido isophthalamide (I) is treated with boric acid and KOH to form the cyclic diborate tripotassium salt (II). Subsequent condensation of (II) with epichlorohydrin (III) yields the dimeric adduct (IV). The borate groups of (IV) are finally removed upon quenching with diluted HCl.

1 Bjoersvik, H.-R.; et al.; A selective process for N-alkylation in competition with O-alkylation: Boric acid, borax, and metaborate as a cheap and effective protecting group applicable for industrial-scale synthetic processes. Org Process Res Dev 2001, 5, 5, 472.
2 Priebe, H. (Amersham plc); An N-alkylation. GB 2331098 .
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) 59311 5-(acetylamino)-N~1~,N~3~-bis(2,3-dihydroxypropyl)-2,4,6-triiodoisophthalamide C16H20I3N3O7 详情 详情
(II) 59314   C16H19B2I3K3N3O11 详情 详情
(III) 10146 Epichlorohydrin; 2-(Chloromethyl)oxirane 106-89-8 C3H5ClO 详情 详情
(IV) 59315   C35H44B4I6K4N6O23 详情 详情
Extended Information