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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1396857생성일: 2026년 10월 25일

Citric Acid → (2R)-3-cyclopentyl-2-({formyl[(phenylmethyl)oxy]amino}methyl)propanoyl fluoride

https://huagongshe.com/reaction/1396857

반응식

참여 물질

역할이름HCID투입량
반응물Citric AcidHCID 311—
반응물PyridineHCID 1049—
반응물Cyanuric fluorideHCID 12664—
반응물(R)-3-(Benzyloxy-formyl-amino)-2-cyclopentylmethyl-propionic acidHCID 21305218—
용매DichloromethaneHCID 6344—
생성물(2R)-3-cyclopentyl-2-({formyl[(phenylmethyl)oxy]amino}methyl)propanoyl fluorideHCID 8670634064.7%

반응 단계

2,4,6-Trifluoro-1,3,5-triazine (10.7 g, 79 mmol) was added into a solution of pyridine (6.4 ml, 79 mmol) and (2R)-3-cyclopentyl-2-({formyl[(phenylmethyl)oxy]amino}methyl)propanoic acid (WO 2009061879) (22 g, 72.0 mmol) in dichloromethane (348 ml) at room temperature. The resulting solution was stirred overnight. Dichloromethane (300 mL) was added to the reaction solution, followed by 1000 mL of 5% citric acid, and the mixture was filtrated. The solids were washed with DCM (300 ml). The organic layer of the filtrate was separated and washed with sat. NaHCO3 (2×300 mL). The organic layer was dried over Na2SO4, filtered and concentrated to yield a yellow oil, which was purified by silica gel chromatography (CombiFlash, Column: 220 g; 0-20% ethyl acetate in hexane; 50 min) to provide (2R)-3-cyclopentyl-2-({formyl[(phenylmethyl)oxy]amino}methyl)propanoyl fluoride (14.32 g, 64.7% yield) as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08901119B2
출처 데이터셋uspto-grants-2014_12
ORD IDord-529b8d9667ae46d48ef4dfaf22d3cf69
출처 메모uspto-grants-2014_12