Dimethylformamide → 3-(7-Hydroxy-2,4-dimethoxy-5,5-dimethyl-5,7-dihydro-furo[3,4-d]pyrimidin-7-yl)-5-methyl-benzonitrile

HRID 426283노트

반응식

HRID 426283 반응식
[C:1]([CH2:3][C:4]1[CH:5]=[C:6]([CH:9]=[C:10]([CH3:12])[CH:11]=1)[C:7]#[N:8])#[N:2].ClC1[C:19]([C:20]([OH:23])([CH3:22])[CH3:21])=[C:18]([O:24][CH3:25])[N:17]=[C:16]([O:26][CH3:27])N=1.[H-].[Na+].CN(C=[O:34])C>>[OH:34][C:3]1([C:4]2[CH:5]=[C:6]([CH:9]=[C:10]([CH3:12])[CH:11]=2)[C:7]#[N:8])[C:1]2[N:2]=[C:16]([O:26][CH3:27])[N:17]=[C:18]([O:24][CH3:25])[C:19]=2[C:20]([CH3:22])([CH3:21])[O:23]1

참가 물질

5

반응 조건

온도
0 °C

실험 절차

3-Cyanomethyl-5-methyl-benzonitrile (0.067 g, 0.432 mmol) and 2-(4-Chloro-2,6-dimethoxy-pyrimidin-5-yl)-propan-2-ol (0.100 g, 0.432 mmol) was dissolved in DMF (1.5 mL) and cooled to 0° C. 60% Sodium hydride (0.035 g, 0.64 mmol) was added portionwise and the reaction was stirred at 0° C. for 1 h, then rt overnight. The reaction was quenched with 1N HCl, extracted with ethyl acetate and washed with saturated ammonium chloride solution. Organic layer was dried (MgSO4) and concentrated and purified by flash column chromatography (silica gel, 0 to 40% ethyl acetate/hexane) to give a white solid (0.027 g, 18%). 1H NMR (300 MHz, CDCl3): δ 7.80 (s, 2H), 7.39 (s, 1H), 4.01 (s, 3H), 3.93 (s, 3H), 2.37 (s, 3H), 1.66 (s, 3H), 1.63 (s, 3H). Mass spectrum: 342.3 (M+H)+.

후처리

  1. customrt overnight
  2. customThe reaction was quenched with 1N HCl
  3. extractionextracted with ethyl acetate
  4. washwashed with saturated ammonium chloride solution
  5. dry with materialOrganic layer was dried (MgSO4)
  6. concentrationconcentrated
  7. custompurified by flash column chromatography (silica gel, 0 to 40% ethyl acetate/hexane)

출처 및 근거

ORD 기록
ord-b167f60d3dbd4584b4886a3d9f0e1443
출처 데이터셋
uspto-grants-2012_01
특허 번호
US08106064B2

반응 노트

불러오는 중…