Potassium Carbonate → 6-(3,5-Dimethoxy-phenyl)-8-ethyl-2-methylsulfanyl-8H-pyrido[2,3-d]pyrimidin-7-ylideneamine

HRID 1793878

반응식

HRID 1793878 반응식
[CH2:1]([NH:3][C:4]1[C:9]([CH:10]=O)=[CH:8][N:7]=[C:6]([S:12][CH3:13])[N:5]=1)[CH3:2].CO[C:16]1[CH:17]=[C:18]([CH2:24][C:25]#[N:26])[CH:19]=[C:20]([O:22][CH3:23])[CH:21]=1.[C:27]([O-:30])([O-])=O.[K+].[K+]>CN(C=O)C>[CH3:23][O:22][C:20]1[CH:19]=[C:18]([C:24]2[C:25](=[NH:26])[N:3]([CH2:1][CH3:2])[C:4]3[N:5]=[C:6]([S:12][CH3:13])[N:7]=[CH:8][C:9]=3[CH:10]=2)[CH:17]=[C:16]([O:30][CH3:27])[CH:21]=1

참가 물질

5

실험 절차

To a solution of the product of Example 3, 4-ethylamino-2-methylsulfanyl-pyrimidine-5-carboxaldehyde (37.0 g, 0.19 mol) and 3,5-dimethoxyphenylacetonitrile (37.0 g, 0.21 mol) in DMF (300 mL) was added portionwise anhydrous K2CO3 (130 g) with stirring. The reaction mixture was heated overnight at 105–110° C. and filtered hot. The insoluble salts were washed with DMF (100 mL), and water was added to the warm filtrate until the solution just turned turbid. Crystals developed upon seeding or inducement (scratching with a glass rod). The product was collected by filtration, washed with 100 mL DMF/H2O (25:75), washed with water, and dried in vacuo to afford 50.5 g (76%) of the titled compound. mp 93–95° C.

후처리

  1. temperatureThe reaction mixture was heated overnight at 105–110° C.
  2. filtrationfiltered hot
  3. washThe insoluble salts were washed with DMF (100 mL), and water
  4. additionwas added to the warm filtrate until the solution just turned turbid
  5. filtrationThe product was collected by filtration
  6. washwashed with 100 mL DMF/H2O (25:75)
  7. washwashed with water
  8. customdried in vacuo

출처 및 근거

ORD 기록
ord-b253223e501e42c8b794043a5caa9902
출처 데이터셋
uspto-grants-2006_04
특허 번호
US07022711B2

연결된 노트

불러오는 중…