【结 构 式】 |
【分子编号】44707 【品名】4-pyridinylboronic acid 【CA登记号】1692-15-5 |
【 分 子 式 】C5H6BNO2 【 分 子 量 】122.91918 【元素组成】C 48.86% H 4.92% B 8.8% N 11.4% O 26.03% |
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)Suzuki coupling of 4-bromonaphth-1-ylamine (I) with 4-pyridylboronic acid (II) furnished 4-(pyridyl)-1-naphthylamine (III), which was further converted into isocyanate (IV) by treatment with triphosgene.
【1】 Evans, M.; Gaster, L.M.; Gordon, l.; et al.; Mixed 5-HT1A/1B/1D receptor antagonists as novel antidepressants. 16th Int Symp Med Chem (Sept 18 2000, Bologna) 2000, Abst PB-77. |
【2】 Gaster, L.M.; Rami, H.K.; Wyman, P.A. (SmithKline Beecham plc); Indole derivs. having combined 5HT1A, 5HT1B and 5HT1D receptor antagonist activity. EP 0975593; WO 9850358 . |
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) | 44706 | 4-bromo-1-naphthalenamine; 4-bromo-1-naphthylamine | C10H8BrN | 详情 | 详情 | |
(II) | 44707 | 4-pyridinylboronic acid | 1692-15-5 | C5H6BNO2 | 详情 | 详情 |
(III) | 44708 | 4-(4-pyridinyl)-1-naphthalenamine; 4-(4-pyridinyl)-1-naphthylamine | C15H12N2 | 详情 | 详情 | |
(IV) | 44709 | 4-(4-pyridinyl)-1-naphthyl isocyanate; 4-(4-isocyanato-1-naphthyl)pyridine | C16H10N2O | 详情 | 详情 |
Extended Information