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【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