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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 983061생성일: 2026년 10월 27일

(S)-2-chlorocarbonyl-pyrrolidine-1-carboxylic acid tert-butyl ester → (S)-2-(5,6,7,8-tetrahydro-1H-pyrrolo[3,2-b]azepine-4-carbonyl)-pyrrolidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/983061

반응식

참여 물질

역할이름HCID투입량
반응물(S)-2-chlorocarbonyl-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 11148997—
반응물1,4,5,6,7,8-Hexahydropyrrolo[3,2-B]azepineHCID 22561790—
용매DichloromethaneHCID 6344—
생성물(S)-2-(5,6,7,8-tetrahydro-1H-pyrrolo[3,2-b]azepine-4-carbonyl)-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 20761536—

반응 단계

To a solution of(S)-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester (664 mg) in DCM (10 mL) at 0° C. was added oxalyl chloride (4.7 mmol), followed by one drop of DMF. After stirring at rt for 2 hours, the solvent was concentrated to give S) 2-chlorocarbonyl-pyrrolidine-1-carboxylic acid tert-butyl ester. To a solution of 1,4,5,6,7,8-hexahydro-pyrrolo[3,2-b]azepine (350 mg, 2.6 mmol) was added TEA (362 μL) and (S)-2-chlorocarbonyl-pyrrolidine-1-carboxylic acid tert-butyl ester (dissolved in 10 mL of DCM). After stirring at rt for overnight, the reaction was diluted with DCM, washed with NaHCO3, brine, dried and concentrated. The residue was purified on a silica gel column to give 410 mg of (S)-2-(5,6,7,8-tetrahydro-1H-pyrrolo[3,2-b]azepine-4-carbonyl)-pyrrolidine-1-carboxylic-acid tert-butyl ester as a light brown liquid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06861418B2
출처 데이터셋uspto-grants-2005_03
ORD IDord-d33a4ec1f8004256b23ff28a66588708
출처 메모uspto-grants-2005_03