Sodium Thiosulfate → (4R,7S)-4-azido-7-(2-methyl-4-nitro-pyrazol-3-yl)oxepan-3-one

HRID 521883노트

반응식

HRID 521883 반응식
[N:1]([C@@H:4]1[CH2:10][CH2:9][C@@H:8]([C:11]2[N:15]([CH3:16])[N:14]=[CH:13][C:12]=2[N+:17]([O-:19])=[O:18])[O:7][CH2:6][C@H:5]1[OH:20])=[N+:2]=[N-:3].CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C=CC=CC1=2)=O.C([O-])(O)=O.[Na+].S([O-])([O-])(=O)=S.[Na+].[Na+]>C(Cl)Cl>[N:1]([C@@H:4]1[CH2:10][CH2:9][C@@H:8]([C:11]2[N:15]([CH3:16])[N:14]=[CH:13][C:12]=2[N+:17]([O-:19])=[O:18])[O:7][CH2:6][C:5]1=[O:20])=[N+:2]=[N-:3]

참가 물질

6

실험 절차

To a solution of (3S,4R,7S)-4-azido-7-(1-methyl-4-nitro-1H-pyrazol-5-yl)oxepan-3-ol (1.4 g, 4.96 mmol, intermediate 90) in DCM (35 mL) was added Dess-Martin peridionane (2.52 g, 5.96 mmol) and the mixture stirred at room temperature for 2 hr. Aqueous saturated NaHCO3 (60 mL) and 20% sodium thiosulfate solution (50 mL) were added and the reaction mixture was stirred for 30 min until full dissolution of salts was observed. The organic layer was separated, dried over MgSO4 and solvents removed under reduced pressure. Purification via silica gel column chromatography (0-40% EtOAc/isoHexane) gave (4R,7S)-4-azido-7-(2-methyl-4-nitro-pyrazol-3-yl)oxepan-3-one as an off-white solid (1.1 g, 82%). 1H NMR (400 MHz, CDCl3) δ 8.05 (s, 1H), 5.38 (dd, J=10.2, 2.7 Hz, 1H), 4.62-4.49 (m, 2H), 4.31-4.22 (m, 1H), 4.08 (s, 3H), 2.31-2.17 (m, 3H), 2.15-2.04 (m, 1H).

후처리

  1. stirringthe reaction mixture was stirred for 30 min until full dissolution of salts
  2. customThe organic layer was separated
  3. dry with materialdried over MgSO4 and solvents
  4. customremoved under reduced pressure
  5. customPurification via silica gel column chromatography (0-40% EtOAc/isoHexane)

출처 및 근거

ORD 기록
ord-601b8b93fbd94f61a1c5df1d5375c2ea
출처 데이터셋
uspto-grants-2016_05
특허 번호
US09328106B2

반응 노트

불러오는 중…