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【结 构 式】

【分子编号】50919

【品名】3-chloro-N-hydroxy-N-(2-propynyl)propanamide

【CA登记号】

【 分 子 式 】C6H8ClNO2

【 分 子 量 】161.58776

【元素组成】C 44.6% H 4.99% Cl 21.94% N 8.67% O 19.8%

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)

Alkylation of hydroxylamine with propargyl bromide (I) provided N-propargyl hydroxylamine (II), which was subsequently acylated with 3-chloropropionyl chloride (III) in the presence of pyridine to yield the N-hydroxy amide (IV). Mannich reaction of the propargyl compound (IV) with paraformaldehyde and pyrrolidine (V) with simultaneous cyclization of the N-hydroxy chloropropionamide furnished the title compound.

1 Amstutz, R.; et al.; Position 5 at the oxotremorinic skeleton as the stearing position for activity at the muscarinic receptors. Helv Chim Acta 1987, 70, 2232.
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) 11176 3-Bromopropyne; 3-Bromo-1-propyne 106-96-7 C3H3Br 详情 详情
(II) 50918 3-(hydroxyamino)-1-propyne; N-(2-propynyl)hydroxylamine C3H5NO 详情 详情
(III) 18935 3,4-dimethoxyphenylamine; 3,4-dimethoxyaniline 6315-89-5 C8H11NO2 详情 详情
(IV) 50919 3-chloro-N-hydroxy-N-(2-propynyl)propanamide C6H8ClNO2 详情 详情
(V) 11376 Pyrrolidine 123-75-1 C4H9N 详情 详情
Extended Information