【结 构 式】 |
【分子编号】56967 【品名】(1S,5R,13R,17S)-14-(benzylimino)-4-(cyclopropylmethyl)-12-oxa-4-azapentacyclo[9.6.1.0~1,13~.0~5,17~.0~7,18~]octadeca-7(18),8,10-triene-10,17-diol 【CA登记号】 |
【 分 子 式 】C27H30N2O3 【 分 子 量 】430.54688 【元素组成】C 75.32% H 7.02% N 6.51% O 11.15% |
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:(II)Condensation of naltrexone (I) with benzylamine produces the intermediate imine (II) which is subsequently cyclized with trans-beta-nitrostyrene (III) to produce the required pyrrolomorphinan.
【1】 Miller, C.N.; Traynor, J.R.; Aceto, M.D.; Husbands, S.M.; Lewis, J.W.; Srivastava, S.K.; 4'-Arylpyrrolomorphinans: Effect of a pyrrolo-N-benzyl substituent in enhancing delta-opioid antagonist activity. J Med Chem 2002, 45, 2, 537. |
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) | 25079 | (1S,5R,13R,17S)-4-(cyclopropylmethyl)-10,17-dihydroxy-12-oxa-4-azapentacyclo[9.6.1.0(1,13).0(5,17).0(7,18)]octadeca-7(18),8,10-trien-14-one; Naltrexone | 16590-41-3 | C20H23NO4 | 详情 | 详情 |
(II) | 56967 | (1S,5R,13R,17S)-14-(benzylimino)-4-(cyclopropylmethyl)-12-oxa-4-azapentacyclo[9.6.1.0~1,13~.0~5,17~.0~7,18~]octadeca-7(18),8,10-triene-10,17-diol | C27H30N2O3 | 详情 | 详情 | |
(III) | 56968 | trans-1-Nitro-2-phenylethylene | 5153-67-3 | C8H7NO2 | 详情 | 详情 |
Extended Information