【结 构 式】 |
【分子编号】49109 【品名】2-(2-hydroxyphenyl)-4H-1,3-benzoxazin-4-one 【CA登记号】 |
【 分 子 式 】C14H9NO3 【 分 子 量 】239.2304 【元素组成】C 70.29% H 3.79% N 5.85% O 20.06% |
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)Cyclization of salicylamide (I) with salicyloyl chloride (II) by heating at 170 oC provides 2-(2-hydroxyphenyl)-benz[e][1,3]oxazin-4-one (III), which is finally cyclized with 4-hydrazinobenzoic acid (IV) in refluxing ethanol.
【1】 Lattmann, R.; Acklin, P. (Novartis AG); Substd. 3,5-diphenyl-1,2,4-triazoles and their use as pharmaceutical metal chelators. EP 0914118; JP 2000507601; WO 9749395 . |
【2】 McIntyre, J.A., Castaner, J., Mealy, N.E., Bayes, M.; Deferasirox. Drugs Fut 2004, 29 (4): 331 |
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) | 14652 | salicylamide | 65-45-2 | C7H7NO2 | 详情 | 详情 |
(II) | 32668 | 2-hydroxybenzoyl chloride | C7H5ClO2 | 详情 | 详情 | |
(III) | 49109 | 2-(2-hydroxyphenyl)-4H-1,3-benzoxazin-4-one | C14H9NO3 | 详情 | 详情 | |
(IV) | 49110 | 4-Carboxyphenyl hydrazine; p-Hydrazinobenzoic acid; p-Carboxyphenyl hydrazine; 4-Hydrazinobenzoic acid | 619-67-0 | C7H8N2O2 | 详情 | 详情 |
Extended Information