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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 279259생성일: 2026년 10월 25일

Formic Acid → (R)-3-[[N-(2-(tert-butoxycarbonylamino)-5-trifluoromethylbenzoyl)glycyl]amino]pyrrolidine

https://huagongshe.com/reaction/279259

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참여 물질

역할이름HCID투입량
반응물Formic AcidHCID 284—
반응물(R)-3-[[N-(2-(tert-butoxycarbonylamino)-5-trifluoromethylbenzoyl)glycyl]amino]-1-(4-chlorobenzyl)pyrrolidineHCID 54203221—
촉매Palladium hydroxideHCID 9942167—
용매MethanolHCID 887—
생성물(R)-3-[[N-(2-(tert-butoxycarbonylamino)-5-trifluoromethylbenzoyl)glycyl]amino]pyrrolidineHCID 5430712990.1%

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온도50 °C

반응 단계

A mixture of (R)-3-[{N-(2-(tert-butoxycarbonylamino)-5-trifluoromethylbenzoyl)glycyl}amino]-1-(4-chlorobenzyl)pyrrolidine (6.3 g, 11.4 mmol), Pd(OH)2 (1.68 g), HCO2H (3.7 mL), and methanol (80 mL) was stirred at 50° C. overnight. After the mixture was cooled to room temperature, the Pd catalyst was filtered off through Celite and the filtrate was concentrated. Column chromatography (SiO2, AcOEt, AcOEt/MeOH=5/1-4/1) gave (R)-3-[{N-(2-(tert-butoxycarbonylamino)-5-trifluoromethylbenzoyl)glycyl}amino]pyrrolidine (4.42 g, 90%) as a white solid: 1H NMR (CDCl3, 400 MHz) δ1.48 (s, 9H), 2.0-2.4 (m, 2H), 3.42-3.71 (m, 5H), 4.00-4.22 (m, 2H), 4.56 (br, 1H), 7.48 (d, J=9.0 Hz, 1H), 7.93 (s, 1H), 8.17 (br, 1H), 8.33 (d, J=9.0 Hz, 1H), 8.45 (br, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06362177B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-70a7d2d4327248a492d3723e0fad1f7f
출처 메모uspto-grants-2002_03