돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1358498생성일: 2026년 10월 27일

Water → 1-[(2S,3R)-2-benzyloxy-5-(2-oxobenzothiazol-3-yl)-3-pentyl]imidazole-4-carboxamide

https://huagongshe.com/reaction/1358498

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물BenzothiazoloneHCID 13625—
반응물Sodium hydrideHCID 24758—
반응물1-[(2S,3R)-2-benzyloxy-5-methanesulfonyloxy-3-pentyl]imidazole-4-carboxamideHCID 11164927—
용매DimethylformamideHCID 6228—
생성물1-[(2S,3R)-2-benzyloxy-5-(2-oxobenzothiazol-3-yl)-3-pentyl]imidazole-4-carboxamideHCID 5701534752.7%

반응 조건

온도65 °C

반응 단계

To a stirred solution of 2-oxobenzothiazole (83 mg, 0.549 mmol) in DMF (3 ml) was added NaH (60% in mineral oil, 22 mg, 0.549 mmol) at room temperature. After 10 minutes, 1-[(2S,3R)-2-benzyloxy-5-methanesulfonyloxy-3-pentyl]imidazole-4-carboxamide in DMF (3 ml) was added and the resulting mixture was stirred for 6 hours at 60 to 70° C. The reaction mixture was poured into water (30 ml) and extracted with ethyl acetate. The organic layer was washed with brine, dried (sodium sulfate), and concentrated in vacuo. The residue was purified by silica gel (8 g) column chromatography eluting with chloroform/methanol (100:1 to 30:1) to give 1-[(2S,3R)-2-benzyloxy-5-(2-oxobenzothiazol-3-yl)-3-pentyl]imidazole-4-carboxamide (63 mg, 52.7%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06596738B1
출처 데이터셋uspto-grants-2003_07
ORD IDord-7d5460f6e3734611b331b2cca7655c92
출처 메모uspto-grants-2003_07