【结 构 式】 |
【分子编号】66567 【品名】1,2,3,4-tetrahydro-1-naphthoic acid 【CA登记号】1914-65-4 |
【 分 子 式 】C11H12O2 【 分 子 量 】176.21508 【元素组成】C 74.98% H 6.86% O 18.16% |
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)
【1】 Robinson JR, Kowalczyk JC. 1996. Process for preparing 2-(l-azabicyclo[2, 2, 2] oct-3-yl)-2,3,3a,4, 5,6-hexahydnrlH-benz [de] isoqui nolin-l-one. US 5510486 |
【1】 Robinson JR, Kowalczyk JC. 1996. Process for preparing 2-(l-azabicyclo[2. 2, 2] oct-3-yl)-2,3,3a,4,5,6-hexahydnrlH-benz [de] isoqui nolin-l-one. US 5510486 |
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) | 16982 | 1H,3H-benzo[de]isochromene-1,3-dione; 1,8-Naphthalic Anhydride | 81-84-5 | C12H6O3 | 详情 | 详情 |
(I) | 66567 | 1,2,3,4-tetrahydro-1-naphthoic acid | 1914-65-4 | C11H12O2 | 详情 | 详情 |
(II) | 16985 | 2-[(3S)-1-azabicyclo[2.2.2]oct-3-yl]-1H-benzo[de]isoquinoline-1,3(2H)-dione | C19H18N2O2 | 详情 | 详情 | |
(II) | 27373 | 1,2,3,4-tetrahydro-1-naphthalenecarbonyl chloride | C11H11ClO | 详情 | 详情 | |
(III) | 16986 | 2-[(3S)-1-azabicyclo[2.2.2]oct-3-yl]-3-hydroxy-2,3,3a,4,5,6-hexahydro-1H-benzo[de]isoquinolin-1-one | C19H24N2O2 | 详情 | 详情 | |
(III) | 16991 | N-[(3S)-1-azabicyclo[2.2.2]oct-3-yl]-5,6,7,8-tetrahydro-1-naphthalenecarboxamide | 135729-78-1 | C18H24N2O | 详情 | 详情 |
(IV) | 16987 | 2-[(3S)-1-azabicyclo[2.2.2]oct-3-yl]-2,4,5,6-tetrahydro-1H-benzo[de]isoquinolin-1-one | C19H22N2O | 详情 | 详情 | |
(IV) | 66568 | (2S)-N-((1,2,3,4-tetrahydronaphthalen-1-yl)methyl)quinuclidin-2-amine | C18H26N2 | 详情 | 详情 |
Extended Information