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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 79689생성일: 2026년 10월 24일

Glycine tert-butyl ester → 5-[(Tert-butoxycarbonylmethyl-amino)-methyl]-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester

https://huagongshe.com/ko/reaction/79689

반응식

참여 물질

역할이름HCID투입량
반응물Glycine tert-butyl esterHCID 151417—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물5-Formyl-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl esterHCID 72338046—
용매DichloromethaneHCID 6344—
생성물5-[(Tert-butoxycarbonylmethyl-amino)-methyl]-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl esterHCID 6662093047.1%

반응 단계

Sodium triacetoxyborohydride (2.08 g, 9.86 mmol) was added to a solution of 5-formyl-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester (891 mg, 3.29 mmol) and glycine t-butyl ester (1.65 g, 9.86 mmol) in dichloromethane (20 mL) over 2 minutes—a small amount of gas evolution was observed. After 1 hour the reaction was quenched with saturated ammonium chloride (5 mL). The mixture was extracted with ethyl acetate (3×25 mL). The combined organic phases were dried over sodium sulfate, filtered and the solvent was removed under reduced pressure. The resulting residue was purified by flash chromatography with methanol and dichloromethane as the eluant at a gradient of 0-10%. The fractions containing product were combined and the solvent was removed under reduced pressure to provide 5-[(tert-butoxycarbonylmethyl-amino)-methyl]-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester (601 mg, 1.55 mmol, 47%). C19H34N2O6 calculated 386.2, observed [M+1]+ 387.2; rt=1.61 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841278B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-009df566ff8b442cbc8d90e62599bb72
출처 메모uspto-grants-2014_09