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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 58818생성일: 2026년 10월 24일

4-Methylmorpholine → (2S,3R)-methyl 3-hydroxy-2-(2-morpholinoacetamido)butanoate

https://huagongshe.com/ko/reaction/58818

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물4-Morpholineacetic acidHCID 438968—
반응물Methyl L-threoninate hydrochlorideHCID 2734893—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
용매DichloromethaneHCID 6344—
생성물(2S,3R)-methyl 3-hydroxy-2-(2-morpholinoacetamido)butanoateHCID 11760820648%

반응 단계

HATU (7.66 g, 20.1 mmol) was added to a solution of 2-morpholinoacetic acid (2.44 g, 16.8 mmol) and (2S,3R)-methyl 2-amino-3-hydroxybutanoate hydrochloride (2.84 g, 16.8 mmol) in dichloromethane (20 mL) at 0° C. N-Methylmorpholine (5.1 g, 50.4 mmol) was added and the reaction mixture was allowed to warm to ambient temperature and stirred for 1 h. The mixture was concentrated and the residue was purified by flash column chromatography on silica gel (dichloromethane/methanol=100:1 to 60:1) to afford (2S,3R)-methyl 3-hydroxy-2-(2-morpholinoacetamido)butanoate (2.1 g, 48% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434761B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-1d62453ce0004896ace76155e6286cbf
출처 메모uspto-grants-2016_09