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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 239091생성일: 2026년 10월 24일

Oxalic Acid → (1R,2S,3R,5R,6R)-2-amino-2-cyano-3-[(3,4-dichloro benzyl)oxy]-6-fluoro bicyclo[3.1.0]hexane-6-carboxamide oxalate

https://huagongshe.com/ko/reaction/239091

반응식

참여 물질

역할이름HCID투입량
반응물Oxalic AcidHCID 971—
반응물(1R,2S,3R,5R,6R)-2-amino-2-cyano-3-[(3,4-dichloro benzyl)oxy]-6-fluoro bicyclo[3.1.0]hexane-6-carboxamideHCID 53236629—
반응물(1R,2R,3R,5R,6R)-2-amino-2-cyano-3-[(3,4-dichloro benzyl)oxy]-6-fluoro bicyclo[3.1.0]hexane-6-carboxamideHCID 68227672—
용매Ethyl AcetateHCID 8857—
생성물(1R,2S,3R,5R,6R)-2-amino-2-cyano-3-[(3,4-dichloro benzyl)oxy]-6-fluoro bicyclo[3.1.0]hexane-6-carboxamide oxalateHCID 68227660—

반응 단계

To ethyl acetate (5 mL) solution containing 251.0 mg of the mixture of (1R,2S,3R,5R,6R)-2-amino-2-cyano-3-[(3,4-dichloro benzyl)oxy]-6-fluoro bicyclo[3.1.0]hexane-6-carboxamide (6a) and (1R,2R,3R,5R,6R)-2-amino-2-cyano-3-[(3,4-dichloro benzyl)oxy]-6-fluoro bicyclo[3.1.0]hexane-6-carboxamide (8a) [containing (6a): 171.5 mg and (8a): 75.1 mg], 67.7 mg (content: 98 wt %) of oxalic acid was added and stirred for 17 hrs and 50 min at room temperature. The resulting slurry was filtered under suction, washed with 2 mL of ethyl acetate, and dried under reduced pressure at room temperature. 217.0 mg of the resulting colorless powder (229.1 mg obtained) was suspended in 2.5 mL of ethyl acetate, and stirred at room temperature for 15.5 hrs. The resulting slurry was filtered under suction, washed with 2 mL of ethyl acetate, and dried under reduced pressure at room temperature to obtain 193.5 mg of (1R,2S,3R,5R,6R)-2-amino-2-cyano-3-[(3,4-dichloro benzyl)oxy]-6-fluorobicyclo[3.1.0]hexane-6-carboxamide oxalate (6d) as a colorless solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642777B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-e89087b9ecd44e4485861a175069ea7a
출처 메모uspto-grants-2014_02