【结 构 式】 |
【分子编号】23392 【品名】7-hydroxy-4a,8a-dihydro-2(1H)-quinolinone 【CA登记号】 |
【 分 子 式 】C9H9NO2 【 分 子 量 】163.176 【元素组成】C 66.25% H 5.56% N 8.58% O 19.61% |
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)The condensation of 7-hydroxycarbostyryl (I) with 1-bromo-3-chloropropane (II) by means of KOH in hot isopropranol gives 7-(3-chloropropoxy)carbostyryl (III), which is then allowed to react with 1-(2,3-dimethylpheny)piperazine (IV) by means of NaI and NaHCO3 in hot acetone.
【1】 Banno, K.; Fujioka, T.; Nakagawa, K.; Oshiro, Y. (Otsuka Pharmaceutical Co., Ltd.); Pharmaceutically useful carbostyril derivs.. DE 2912105; FR 2421174; US 4734416 . |
【2】 Prous, J.; Castaner, J.; OPC-4392. Drugs Fut 1988, 13, 10, 931. |
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) | 23392 | 7-hydroxy-4a,8a-dihydro-2(1H)-quinolinone | C9H9NO2 | 详情 | 详情 | |
(II) | 10358 | 1-Bromo-3-chloropropane | 109-70-6 | C3H6BrCl | 详情 | 详情 |
(III) | 23394 | 7-(3-chloropropoxy)-4a,8a-dihydro-2(1H)-quinolinone | C12H14ClNO2 | 详情 | 详情 | |
(IV) | 23395 | 1-(2,3-dimethylphenyl)piperazine | 1013-22-5 | C12H18N2 | 详情 | 详情 |
Extended Information