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2-(benzyloxy)-5-(4-fluorophenyl)-6,7-dihydropyrazolo[1,5-a]pyrazin-4(5H)-one → HCID 178515148, 화합물

HRID 1396504
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HRID 1396504 반응식
C([O:8][C:9]1[CH:25]=[C:12]2[C:13](=[O:24])[N:14]([C:17]3[CH:22]=[CH:21][C:20]([F:23])=[CH:19][CH:18]=3)[CH2:15][CH2:16][N:11]2[N:10]=1)C1C=CC=CC=1>CCOC(C)=O.CN(C=O)C.[OH-].[OH-].[Pd+2]>[F:23][C:20]1[CH:19]=[CH:18][C:17]([N:14]2[CH2:15][CH2:16][N:11]3[N:10]=[C:9]([OH:8])[CH:25]=[C:12]3[C:13]2=[O:24])=[CH:22][CH:21]=1
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참가 물질

5

반응물 1

HCID 727147832-(benzyloxy)-5-(4-fluorophenyl)-6,7-dihydropyrazolo[1,5-a]pyrazin-4(5H)-one

생성물 1

HCID 178515148HCID 178515148, 화합물수율 88.2%

시약·촉매·용매 3

HCID 9942167Palladium hydroxide촉매HCID 6228Dimethylformamide용매HCID 8857Ethyl Acetate용매

실험 절차

A solution of 2-(benzyloxy)-5-(4-fluorophenyl)-6,7-dihydropyrazolo[1,5-a]pyrazin-4(5H)-one (0.79 g, 2.34 mmol) in a mixture of AcOEt (30 mL) and DMF (30 mL) was hydrogenated in a H-Cube reactor (1.5 ml/min, 70 mm Pd(OH)2/C cartridge, full H2 mode, 80° C., 1 cycle). The solvents were evaporated in vacuo to yield 5-(4-fluorophenyl)-2-hydroxy-6,7-dihydropyrazolo[1,5-a]pyrazin-4(5H)-one (0.51 g, 88% yield) as a white solid, that was used in the next step without further purification.

후처리

  1. customwas hydrogenated in a H-Cube reactor
  2. customThe solvents were evaporated in vacuo

출처 및 근거

ORD 기록
ord-5f5fc78bbe05440da31705de3b2fbcb1
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08901125B2

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