Potassium Carbonate → (3-methyl-1-(2-(1-methyl-1H-indol-5-ylamino)pyrimidin-4-yl)-1H-pyrazol-4-yl)methanol

HRID 539895노트

반응식

HRID 539895 반응식
C[CH:2]([C:4]1[C:5]([CH3:16])=[N:6][N:7]([C:9]2[CH:14]=[CH:13][N:12]=[C:11](Cl)[N:10]=2)[CH:8]=1)[OH:3].[CH3:17][N:18]1[C:26]2[C:21](=[CH:22][C:23]([NH2:27])=[CH:24][CH:25]=2)[CH:20]=[CH:19]1.C(=O)([O-])[O-].[K+].[K+].CC1(C)C2C=CC=C(P(C3C=CC=CC=3)C3C=CC=CC=3)C=2OC2C1=CC=CC=2P(C1C=CC=CC=1)C1C=CC=CC=1>C([O-])(=O)C.[Pd+2].C([O-])(=O)C.O1CCOCC1>[CH3:16][C:5]1[C:4]([CH2:2][OH:3])=[CH:8][N:7]([C:9]2[CH:14]=[CH:13][N:12]=[C:11]([NH:27][C:23]3[CH:22]=[C:21]4[C:26](=[CH:25][CH:24]=3)[N:18]([CH3:17])[CH:19]=[CH:20]4)[N:10]=2)[N:6]=1

참가 물질

7

반응 조건

온도
100 °C

실험 절차

A round bottomed flask was charged with methyl (1-(2-chloropyrimidin-4-yl)-3-methyl-1H-pyrazol-4-yl)methanol (400 mg, 1.78 mmol), 1-methyl-1H-indol-5-amine (338 mg, 1.3 equiv.), potassium carbonate (0.74 g, 3.0 equiv), palladium acetate (40 mg, 0.1 equiv), (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (Xantphos, 206 mg, 0.2 equiv.) and 40 mL of anhydrous dioxane. After being degassed by nitrogen bubbling, the reaction mixture was heated at 100° C. for 12 hours. Volatiles were removed in vacuo and then the resulting residue was extracted with ethyl acetate. The collected organic layer was dried over anhydrous sodium sulfate and then concentrated in vacuo. The resulting residue was purified by recrystallization in acetonitrile to give 241 mg (36%) of the desired product as a brown solid. MS (ESI) m/z 335 [M+H]+.

후처리

  1. customAfter being degassed by nitrogen bubbling
  2. customVolatiles were removed in vacuo
  3. extractionthe resulting residue was extracted with ethyl acetate
  4. dry with materialThe collected organic layer was dried over anhydrous sodium sulfate
  5. concentrationconcentrated in vacuo
  6. customThe resulting residue was purified by recrystallization in acetonitrile

출처 및 근거

ORD 기록
ord-118ac1641f814d1089209b3e5e601e46
출처 데이터셋
uspto-grants-2014_10
특허 번호
US08871778B2

반응 노트

불러오는 중…