【结 构 式】 |
【分子编号】22275 【品名】3-(4-fluorophenyl)-5-hydroxy-4-[4-(methylsulfonyl)phenyl]-2(5H)-furanone 【CA登记号】 |
【 分 子 式 】C17H13FO5S 【 分 子 量 】348.3516232 【元素组成】C 58.62% H 3.76% F 5.45% O 22.96% S 9.21% |
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)Cyclization of hydroxyfuranone (I) with hydrazine in refluxing EtOH produced the pyridazinone (II), which was subsequently alkylated with cyclopropylmethyl bromide (III) in the presence of NaOH to afford the title compound.
【1】 Therien, M.; Li, C.S.; Lau, C.K.; Prasit, P.; Gauthier, J.Y. (Merck Frosst Canada Inc.); Pyridazinones as inhibitors of cyclooxygenase-2. EP 0975604; US 6004960; WO 9841511 . |
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) | 22275 | 3-(4-fluorophenyl)-5-hydroxy-4-[4-(methylsulfonyl)phenyl]-2(5H)-furanone | C17H13FO5S | 详情 | 详情 | |
(II) | 22276 | 4-(4-fluorophenyl)-5-[4-(methylsulfonyl)phenyl]-3(2H)-pyridazinone | C17H13FN2O3S | 详情 | 详情 | |
(III) | 22277 | Cyclopropyl bromide; 1-(Bromomethyl)cyclopropane | 7051-34-5 | C4H7Br | 详情 | 详情 |
Extended Information