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HRID 547276作成日:2026年10月25日

Acetic Acid → HCID 86596000、化合物

https://huagongshe.com/reaction/547276

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物O-(4-chloro-3-trifluoromethyl-benzyl)-hydroxylamineHCID 67189157—
反応物HCID 67191845HCID 67191845—
溶媒MethanolHCID 887—
生成物HCID 86596000HCID 86596000—

反応手順

To a solution of 3-[(6-acetyl-2-ethyl-pyridin-3-ylmethyl)-amino]-propionic acid tert-butyl ester (1 eq) in methanol is added O-(4-chloro-3-trifluoromethyl-benzyl)-hydroxylamine (1 eq) followed by the addition of acetic acid (0.05 eq). The mixture is stirred at room temperature for 5 hours. After concentration, the residue is purified by column chromatography to give 3-({6-[1-(4-cyclohexyl-3-trifluoromethyl-benzyloxyimino)-ethyl]-2-ethyl-pyridin-3-ylmethyl}-amino)-propionic acid tert-butyl ester. MS: (ES+) 562.3 (M+1)+. The tert-butyl group is subsequently removed by treatment with TFA/DCM (1/1) at room temperature. The final compound 3-({6-[1-(4-cyclohexyl-3-trifluoromethyl-benzyloxyimino)-ethyl]-2-ethyl-pyridin-3-ylmethyl}-amino)-propionic acid is purified by preparative LCMS. 1H NMR (400 MHz, CD3OD) δ 1.30-1.62 (m, 8H), 1.72-1.91 (m, 5H), 2.36 (s, 3H), 2.78 (t, 2H), 2.94 (m, 3H), 3.37 (t, 2H), 4.42 (s, 2H), 5.29 (s, 2H), 7.51-7.80 (m, 5H). MS: (ES+): 506.3 (M+1)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07939519B2
出典データセットuspto-grants-2011_05
ORD IDord-3ad63fefedfd41819641a53faa74f213
出典メモuspto-grants-2011_05