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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 986988생성일: 2026년 10월 24일

Water → (1-(2-(3a(r)-Benzyl-2-methyl-3-oxo-2,3,3a,4,6,7-hexahydro-pyrazolo[4,3-c]pyridin-5-yl)-1(r)-benzyloxymethyl-2-oxo-ethylcarbamoyl)-1-methyl-ethyl)-carbamic acid tert-butyl ester

https://huagongshe.com/ko/reaction/986988

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물TartrateHCID 119400—
반응물3a-(r)-Benzyl-2-methyl-2,3a,4,5,6,7-hexahydro-pyrazolo[4,3-c]pyridin-3-oneHCID 9977873—
반응물3-Benzyloxy-2-(2-tert-butoxycarbonylamino-2-methyl-propionylamino)-propionic acidHCID 12967000—
용매HexaneHCID 8058—
용매Ethyl AcetateHCID 8857—
생성물(1-(2-(3a(r)-Benzyl-2-methyl-3-oxo-2,3,3a,4,6,7-hexahydro-pyrazolo[4,3-c]pyridin-5-yl)-1(r)-benzyloxymethyl-2-oxo-ethylcarbamoyl)-1-methyl-ethyl)-carbamic acid tert-butyl esterHCID 1123881574.3%

반응 조건

온도0 °C

반응 단계

To a solution of 3a-(R)-benzyl-2-methyl-2,3a,4,5,6,7-hexahydro-pyrazolo[4,3-c]pyridin-3-one, L-tartrate (10.81 g, 0.0275 mol) in ethyl acetate (216.2 mL) at about −66° C. was added TEA (8.43 mL, 0.0605 mol). The mixture was stirred for about 1.5 hours. After removal of the precipitated salt by filtration, 3-benzyloxy-2-(2-tert-butoxycarbonylamino-2-methyl-propionylamino)-propionic acid (8.7 g, 0.0229 mol) and TEA (19.15 mL, 0.1374 mol) were added at about −35° C., followed by the dropwise addition of 50% PPAA in ethyl acetate (27.5 mL, 0.0458 mol). The mixture was stirred for about 2 hours at about −20° C. to about −27° C., then 1.5 hours while the temperature was slowly raised to about 0° C. The reaction mixture was poured into water and extracted with IPE, washed with 7% NaCl solution and concentrated in vacuo. The crude oil that was obtained was treated with IPE/hexane (50/50) to allow crystallization. The product was obtained as a white solid (10.3 g, yield 74.3%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06630487B2
출처 데이터셋uspto-grants-2003_10
ORD IDord-453de6908a324fb8a3d72c5ade8fbcce
출처 메모uspto-grants-2003_10