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HRID 471118作成日:2026年10月27日

Triethylamine → Ethyl 2-(cyclobutanecarboxamido)-3-mercaptopropanoate

https://huagongshe.com/reaction/471118

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Cyclobutanecarboxylic acidHCID 19494—
反応物Propylphosphonic anhydrideHCID 111923—
反応物Ethyl 2-amino-3-mercaptopropanoate hydrochlorideHCID 6432754—
溶媒DimethylformamideHCID 6228—
生成物Ethyl 2-(cyclobutanecarboxamido)-3-mercaptopropanoateHCID 57989145—

反応手順

Triethylamine (15 mL) was added to a suspension of cyclobutanecarboxylic acid (2.57 mL) and ethyl 2-amino-3-mercaptopropanoate hydrochloride (5 g) in DMF (40 mL). The resulting mixture was cooled in an ice bath and a solution of T3P (1.57M in THF, 20.6 mL) was added dropwise. The resulting mixture was allowed to warm to RT and stirred overnight. The reaction was quenched with saturated sodium bicarbonate solution (50 mL) and the layers separated. The aqueous phase was extracted with DCM (2×100 mL). The combined organic solutions were washed with brine (100 mL), dried over sodium sulphate, filtered and evaporated. The resulting white solid was purified by silica gel chromatography eluting with 4:1 to 1:1 isohexane:ethyl acetate gradient. The fractions containing product were combined and evaporated to give the subtitled compound as a clear oil. Yield 3.20 g.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08629271B2
出典データセットuspto-grants-2014_01
ORD IDord-e27398f9294b4c79a7eb6d97f5dcfd91
出典メモuspto-grants-2014_01