돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 501724생성일: 2026년 10월 26일

Barium hydroxide, monohydrate → (2R,3S)-3-amino-4-(3,5-difluorophenyl)-1-(2-(pent-4-enyl)-5-(trifluoromethyl)-benzylamino)butan-2-ol

https://huagongshe.com/reaction/501724

반응식

참여 물질

역할이름HCID투입량
반응물Barium hydroxide, monohydrateHCID 17749100—
반응물Benzyl (2s,3r)-1-(3,5-difluorophenyl)-3-hydroxy-4-(2-(pent-4-enyl)-5-(trifluoromethyl)benzylamino)butan-2-ylcarbamate trifluoroacetate saltHCID 86622348—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
생성물(2R,3S)-3-amino-4-(3,5-difluorophenyl)-1-(2-(pent-4-enyl)-5-(trifluoromethyl)-benzylamino)butan-2-olHCID 59423701113%

반응 조건

온도110 °C

반응 단계

Step AM (2): To a solution of benzyl (2S,3R)-1-(3,5-difluorophenyl)-3-hydroxy-4-(2-(pent-4-enyl)-5-(trifluoromethyl)benzylamino)butan-2-ylcarbamate trifluoroacetate salt (88 mg, 0.128 mmol) in DME (9.0 mL) and water (6.0 mL) was added barium hydroxide monohydrate (852 mg, 4.5 mmol). The reaction mixture was stirred at 110° C. in a high pressure vial for 18 h. The reaction mixture was filtered through a pad of celite and the filtrate was concentrated in vacuum. The residue was purified by reverse phase chromatography to give (2R,3S)-3-amino-4-(3,5-difluorophenyl)-1-(2-(pent-4-enyl)-5-(trifluoromethyl)-benzylamino)butan-2-ol double trifluoro-acetate salt (64 mg, 74%) as a colorless oil. LC-MS (M+H)+=443.36.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07772221B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-8d85c3f3950e48f08a6fc2c4cbfe9edd
출처 메모uspto-grants-2010_08