【结 构 式】 |
【分子编号】64961 【品名】(5-methyl-2-pyridinyl)methanamine; (5-methyl-2-pyridinyl)methylamine 【CA登记号】 |
【 分 子 式 】C7H10N2 【 分 子 量 】122.16988 【元素组成】C 68.82% H 8.25% N 22.93% |
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:(IV)In an alternative, shorter route, 1-(3-chloro-4-fluorobenzoyl)-4-piperidinone (I) is subjected to Darzens condensation with chloroacetonitrile in the presence of NaOH and a phase-transfer catalyst to furnish the epoxy nitrile (II). Epoxide opening in (II) with HF-pyridine gives rise to the fluoro hydroxy nitrile (III). This is finally condensed with (5-methylpyridin-2-yl)methylamine (IV) under reductive amination conditions to produce the title compound.
【1】 Bonnaud, B.; Maurel, J.-L.; Vacher, B.; Ribet, J.-P. (Pierre Fabre Medicament); Synthesis method and intermediates of pyridin-2-yl-methylamine. WO 0264585 . |
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) | 24372 | 1-(3-chloro-4-fluorobenzoyl)-4-piperidinone | C12H11ClFNO2 | 详情 | 详情 | |
(II) | 64959 | 6-(3-chloro-4-fluorobenzoyl)-1-oxa-6-azaspiro[2.5]octane-2-carbonitrile | C14H12ClFN2O2 | 详情 | 详情 | |
(III) | 64960 | 2-[1-(3-chloro-4-fluorobenzoyl)-4-fluoro-4-piperidinyl]-2-hydroxyacetonitrile | C14H13ClF2N2O2 | 详情 | 详情 | |
(IV) | 64961 | (5-methyl-2-pyridinyl)methanamine; (5-methyl-2-pyridinyl)methylamine | C7H10N2 | 详情 | 详情 |
Extended Information