Cesium carbonate → (4-((5-(4-hydroxyphenyl)-1H-pyrazol-1-yl)methyl)phenyl)(pyrrolidin-1-yl)methanone

HRID 1399810노트

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HRID 1399810 반응식
Br[C:2]1[N:6]([CH2:7][C:8]2[CH:13]=[CH:12][C:11]([C:14]([N:16]3[CH2:20][CH2:19][CH2:18][CH2:17]3)=[O:15])=[CH:10][CH:9]=2)[N:5]=[CH:4][CH:3]=1.[OH:21][C:22]1[CH:27]=[CH:26][C:25](B(O)O)=[CH:24][CH:23]=1.C([O-])([O-])=O.[Cs+].[Cs+]>O1CCOCC1.O.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2]>[OH:21][C:22]1[CH:27]=[CH:26][C:25]([C:2]2[N:6]([CH2:7][C:8]3[CH:13]=[CH:12][C:11]([C:14]([N:16]4[CH2:20][CH2:19][CH2:18][CH2:17]4)=[O:15])=[CH:10][CH:9]=3)[N:5]=[CH:4][CH:3]=2)=[CH:24][CH:23]=1

참가 물질

6

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온도
140 °C

실험 절차

To a solution of (4-((5-bromo-1H-pyrazol-1-yl)methyl)phenyl)(pyrrolidin-1-yl)methanone (231 mg, 0.7 mmol) in dioxane:water (5:1, 25 ml) was added (4-hydroxyphenyl)boronic acid (207 mg, 1.5 mmol), Cs2CO3 (487 mg, 1.5 mmol) and Pd(dppf)Cl2 (86 mg) and the mixture purged with nitrogen. The mixture was then stirred at 140° C. under microwave mediated heating irradiation for 40 min. The mixture was diluted with water, extracted with ethyl acetate three times and the organic layer dried over Na2SO4 before concentration. The crude product was then purified by column chromatography to yield the desired product (173 mg, yield 70%). LCMS (m/z): 348.2 [M+H]+

후처리

  1. customthe mixture purged with nitrogen
  2. temperaturemediated heating
  3. customirradiation for 40 min
  4. additionThe mixture was diluted with water
  5. extractionextracted with ethyl acetate three times
  6. dry with materialthe organic layer dried over Na2SO4 before concentration
  7. customThe crude product was then purified by column chromatography

출처 및 근거

ORD 기록
ord-6aebc4b4fb1c4d0780f3301a3a41f95c
출처 데이터셋
uspto-grants-2014_12
특허 번호
US08906900B2

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