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Cesium carbonate → 5-(4-(1H-pyrazol-1-yl)phenylamino)-7-(cyclopropylamino)-2-methylpyrazolo[1,5-a]pyrimidine-3-carbaldehyde

HRID 624814
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HRID 624814 반응식
[N:1]1([C:6]2[CH:12]=[CH:11][C:9]([NH2:10])=[CH:8][CH:7]=2)[CH:5]=[CH:4][CH:3]=[N:2]1.C([O-])([O-])=O.[Cs+].[Cs+].Cl[C:20]1[CH:25]=[C:24]([N:26]([CH:34]2[CH2:36][CH2:35]2)C(=O)OC(C)(C)C)[N:23]2[N:37]=[C:38]([CH3:42])[C:39]([CH:40]=[O:41])=[C:22]2[N:21]=1.C1C=CC(P(C2C(C3C(P(C4C=CC=CC=4)C4C=CC=CC=4)=CC=C4C=3C=CC=C4)=C3C(C=CC=C3)=CC=2)C2C=CC=CC=2)=CC=1>O1CCOCC1.C([O-])(=O)C.[Pd+2].C([O-])(=O)C.CCOCC>[N:1]1([C:6]2[CH:7]=[CH:8][C:9]([NH:10][C:20]3[CH:25]=[C:24]([NH:26][CH:34]4[CH2:35][CH2:36]4)[N:23]4[N:37]=[C:38]([CH3:42])[C:39]([CH:40]=[O:41])=[C:22]4[N:21]=3)=[CH:11][CH:12]=2)[CH:5]=[CH:4][CH:3]=[N:2]1
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참가 물질

8

반응물 4

HCID 10796Cesium carbonateHCID 5942744-(1H-Pyrazol-1-yl)anilineHCID 634876Binap, (A+-)-HCID 86654658Tert-butyl 5-chloro-3-formyl-2-methylpyrazolo[1,5-a]pyrimidin-7-yl(cyclopropyl)carbamate

생성물 1

HCID 583140345-(4-(1H-pyrazol-1-yl)phenylamino)-7-(cyclopropylamino)-2-methylpyrazolo[1,5-a]pyrimidine-3-carbaldehyde수율 23%

시약·촉매·용매 3

HCID 167845palladium(II) acetate촉매HCID 3283Diethyl Ether용매HCID 312751,4-Dioxane용매

실험 절차

To 4-(1H-pyrazol-1-yl)aniline (54 mg, 0.34 mmol), Cs2CO3 (130 mg, 0.4 mmol) were added to tert-butyl 5-chloro-3-formyl-2-methylpyrazolo[1,5-a]pyrimidin-7-yl(cyclopropyl)carbamate (100 mg, 0.29 mmol) dissolved in 1,4-dioxane (1.1 mL). Racemic BINAP (11 mg, 0.017 mmol) and palladium(II) acetate (8 mg, 0.011 mmol) were then added. The mixture was sealed and irradiated at 110° C. for 60 min in the microwave. Et2O (3 mL) was added and the solution was filtered. The filtrate was concentrated in vacuo. The crude residue was dissolved in dichloromethane (1.5 mL) and trifluoroacetic acid (1.5 mL). After stirring at room temperature for 1 hour, the solution was concentrated under a stream of air. The crude material was purified by silica gel chromatography (15% acetone/dichloromethane) to yield the product, 5-(4-(1H-pyrazol-1-yl)phenylamino)-7-(cyclopropylamino)-2-methylpyrazolo[1,5-a]pyrimidine-3-carbaldehyde (24 mg, 23% yield). LCMS (M+1=374)

후처리

  1. customThe mixture was sealed
  2. customirradiated at 110° C. for 60 min in the microwave
  3. filtrationthe solution was filtered
  4. concentrationThe filtrate was concentrated in vacuo
  5. dissolutionThe crude residue was dissolved in dichloromethane (1.5 mL)
  6. concentrationthe solution was concentrated under a stream of air
  7. customThe crude material was purified by silica gel chromatography (15% acetone/dichloromethane)

출처 및 근거

ORD 기록
ord-f90e9dda2a5f479c845f96602912b8f3
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09303033B2

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