돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 877589생성일: 2026년 10월 25일

Diisobutylaluminum hydride → (6-Chloro-4-(isopropylamino)pyridin-3-yl)methanol

https://huagongshe.com/reaction/877589

반응식

참여 물질

역할이름HCID투입량
반응물Diisobutylaluminum hydrideHCID 14487—
반응물Ethyl 6-chloro-4-(cyclobutylamino)nicotinateHCID 89689654—
용매DichloromethaneHCID 6344—
생성물(6-Chloro-4-(isopropylamino)pyridin-3-yl)methanolHCID 89689798—

반응 조건

온도-78 °C

반응 단계

To a stirred solution of ethyl 6-chloro-4-(isopropylamino)nicotinate (2) (1 g, 4.12 mmol) in dry DCM (30 mL), DIBAL-H (8.24 mmol, 2 equiv.) (1.0 M in DCM) was added dropwise at −78° C. The reaction mixture was stirred at −78° C. for 2 h, gradually, the reaction was allowed to warm up to −10° C. over 1 h. The reaction mixture was quenched with saturated solution of sodium potassium tarterate and allowed to stir at room temperature. The reaction mixture was filtered through a small pad of celite. The filtrate was washed with brine solution, dried over Na2SO4, filtered and concentrated to give crude alcohol. The crude material obtained was purified by flash column chromatography through silica gel and MeOH: CHCl3 as eluent to afford (6-chloro-4-(isopropylamino)pyridin-3-yl)methanol. LC/MS: ZORBAX SB C18, 4.6×50 mm, 5 μm; Solvent A=10% MeOH: 90% H2O: 0.1% TFA; Solvent B=90% MeOH: 10% H2O: 0.1% TFA; gradient 0-100% B over 2 min (3 min run time); retention time: 0.806 min; LCMS (ES-API), m/z 201.0 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08987311B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-e8b67b09633f4dc4a3c5cdb0752e52e5
출처 메모uspto-grants-2015_03