돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 577983생성일: 2026년 10월 25일

Benzaldehyde → {3-(benzylamino)-6-[(2R,6S)-2,6-dimethylmorpholin-4-yl]-7-fluoro-1,2-benzoxazol-5-yl}methanol

https://huagongshe.com/reaction/577983

반응식

참여 물질

역할이름HCID투입량
반응물BenzaldehydeHCID 240—
반응물TriethylsilaneHCID 12052—
반응물{3-amino-6-[(2R,6S)-2,6-dimethylmorpholin-4-yl]-7-fluoro-1,2-benzisoxazol-5-yl}methanolHCID 67359017—
용매Trifluoroacetic acidHCID 6422—
생성물{3-(benzylamino)-6-[(2R,6S)-2,6-dimethylmorpholin-4-yl]-7-fluoro-1,2-benzoxazol-5-yl}methanolHCID 67356861—

반응 단계

To an ice cooled solution of benzaldehyde (0.08 mL, 2.54 mmol) in TFA (5 mL) was added triethylsilane (0.4 mL, 2.5 mmol) followed by {3-amino-6-[(2R,6S)-2,6-dimethylmorpholin-4-yl]-7-fluoro-1,2-benzisoxazol-5-yl}methanol (Intermediate 7, 250 mg, 0.84 mmol), and slowly allowed to reach room temperature and stirred for 12 hour. The reaction mixture was concentrated and the residue thus obtained was purified column chromatography using EtOAc in petether to give the title compound as solid. Yield: 70 mg (21%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09040528B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-0b4b1d40b9364a90b234cef80e703a5d
출처 메모uspto-grants-2015_05