Diisopropylethylamine → (S)-methyl 2-(2,6-dichloropyrimidine-4-carboxamido)propanoate

To a mixture of (S)-methyl 2-aminopropanoate hydrochloride (1.397 g, 10.01 mmol) in DCM (80 mL) was added iPr2NEt (4.35 mL, 24.97 mmol). The mixture was stirred for a few minutes and a solution of the 2,6-dichloropyrimidine-4-carbonyl chloride (2.107 g, 9.97 mmol) in DCM (20 mL) was added over a period of 1 minute. After stirring overnight, the reaction was concentrated in vacuo to a residue. The residue was chromatographed over silica gel using 10-40% EtOAc in hexanes. The product fractions were evaporated in vacuo to give (S)-methyl 2-(2,6-dichloropyrimidine-4-carboxamido)propanoate as a yellow oil (0.921 g, 3.31 mmol, 33% yield). LC/MS: m/z=278.1 [M+H]+.

1. stirringAfter stirring overnight
2. concentrationthe reaction was concentrated in vacuo to a residue
3. customThe residue was chromatographed over silica gel using 10-40% EtOAc in hexanes
4. customThe product fractions were evaporated in vacuo

ORD-Eintrag

ord-2fbadfe6322e495da162beab7ccf6a46

Quelldatensatz

uspto-grants-2015_09

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US09133131B2