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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 643812생성일: 2026년 10월 26일

1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride → tert-butyl L-prolinate

https://huagongshe.com/reaction/643812

반응식

참여 물질

역할이름HCID투입량
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물5-[(4-Phenylphenoxy)methyl]furan-2-carboxylic acidHCID 4683153—
반응물tert-butyl (2R)-pyrrolidine-2-carboxylate hydrochlorideHCID 44629909—
용매TetrahydrofuranHCID 8028—
생성물tert-butyl L-prolinateHCID 10288461.1%

반응 단계

A solution of 5-(biphenyl-4-yloxymethyl)-furan-2-carboxylic acid (of Intermediate 8; 0.134 g, 0.46 mmol), D-proline tert-butyl ester hydrochloride (Bachem; 0.22 g, 1.1 mmol), 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride (Avocado; 0.18 g, 0.95 mmol), and N,N-dimethylaminopyridine (0.166 g, 1.36 mmol) in tetrahydrofuran (10 mL) was stirred at room temperature for 16 h. The solvents were evaporated under reduced pressure, and water and ethyl acetate were added. The aqueous phase was extracted three times with ethyl acetate, and the combined organic layers were dried (sodium sulfate), filtered, evaporated, and purified using a Biotage Flash 40 purification system, eluting with methylene chloride/acetone 9:1, to give 5-(biphenyl-4-yloxymethyl)-furan-2-carbonyl]-D-pyrrolidine-2-carboxylic acid tert-butyl ester as a white solid (0.115 g, 56%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07700632B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-4b55ed77f1a04cefaed8fcc07fbb4178
출처 메모uspto-grants-2010_04