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【结 构 式】

【分子编号】64810

【品名】N-(4-piperidinyl)acetamide

【CA登记号】

【 分 子 式 】C7H14N2O

【 分 子 量 】142.20104

【元素组成】C 59.13% H 9.92% N 19.7% O 11.25%

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:(III)

Acylation of 4-amino-1-benzylpiperidine (I) with acetyl chloride provides the amide (II). Subsequent debenzylation of (II) by transfer hydrogenation with ammonium formate in the presence of Pd/C yields the piperidine (III), which is finally acylated with 4-fluorobenzenesulfonyl chloride (IV) to give the corresponding sulfonamide.

1 Manetti, D.; Martini, E.; Ghelardini, C.; Dei, S.; Galeotti, N.; Guandalini, L.; Romanelli, M.N.; Scapecchi, S.; Teodori, E.; Bartolini, A.; Gualtieri, F.; 4-Aminopiperidine derivatives as a new class of potent cognition enhancing drugs. Bioorg Med Chem Lett 2003, 13, 14, 2303.
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) 34808 1-Benzyl-4-piperidinylamine; 1-Benzyl-4-piperidinamine; 4-Amino-1-benzylpiperidine 50541-93-0 C12H18N2 详情 详情
(II) 64809 N-[1-(phenylmethyl)-4-piperidinyl]acetamide C14H20N2O 详情 详情
(III) 64810 N-(4-piperidinyl)acetamide C7H14N2O 详情 详情
(IV) 12292 4-Fluorobenzenesulfonyl chloride 349-88-2 C6H4ClFO2S 详情 详情
Extended Information