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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1280949생성일: 2026년 10월 24일

Triethylamine → (R)-1-(4-chlorobenzyl)-3-[[N-(4-dimethylaminobenzoyl)glycyl]amino]pyrrolidine

https://huagongshe.com/ko/reaction/1280949

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-(Dimethylamino)benzoic acidHCID 12092—
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물(R)-1-(4-chlorobenzyl)-3-(glycylamino)pyrrolidineHCID 54551710—
용매ChloroformHCID 6212—
생성물(R)-1-(4-chlorobenzyl)-3-[[N-(4-dimethylaminobenzoyl)glycyl]amino]pyrrolidineHCID 69215736—

반응 단계

A solution of (R)-1-(4-chlorobenzyl)-3-(glycylamino)pyrrolidine (13.8 mg, 0.052 mmol) in CHCl3 (2 mL) was treated with Et3N (0.021 mL, 0.15 mmol), 4-(dimethylamino)benzoic acid (10 mg, 0.061 mmol), EDCI (10.2 mg, 0.053 mmol) and HOBt (7.5 mg, 0.055 mmol). The reaction mixture was stirred at room temperature for 16 h. The solution was washed with 2 N aqueous NaOH solution (2 mL×2) and brine (2 mL), and dried by filtration through a PTFE membrane using CH2Cl2 (3 mL). Concentration afforded the desired material (compound No. 952) (24.9 mg, quant): The purity was determined by RPLC/MS (91%); ESI/MS m/e 415.0 (M++H, C22H27ClN4O2).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06451842B1
출처 데이터셋uspto-grants-2002_09
ORD IDord-c1216aed88664c66a1c17263040677a0
출처 메모uspto-grants-2002_09