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Ammonium formate → 7-hydroxy-5-isopropoxyquinazolin-4(3H)-one

HRID 639981
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반응식

HRID 639981 반응식
C([O-])=O.[NH4+].C([O:12][C:13]1[CH:22]=[C:21]2[C:16]([C:17](=[O:23])[NH:18][CH:19]=[N:20]2)=[C:15]([O:24][CH:25]([CH3:27])[CH3:26])[CH:14]=1)C1C=CC=CC=1>[Pd].CN(C)C=O>[OH:12][C:13]1[CH:22]=[C:21]2[C:16]([C:17](=[O:23])[NH:18][CH:19]=[N:20]2)=[C:15]([O:24][CH:25]([CH3:27])[CH3:26])[CH:14]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 2723923Ammonium formateHCID 1355106847-(benzyloxy)-5-isopropoxyquinazolin-4(3H)-one

생성물 1

HCID 1363551707-hydroxy-5-isopropoxyquinazolin-4(3H)-one수율 100%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 6228Dimethylformamide용매

실험 절차

Ammonium formate (9.5 g, 150 mmol) and 10% palladium on carbon (500 mg) were added to a solution of 7-(benzyloxy)-5-isopropoxyquinazolin-4(3H)-one (4.6 g, 15.0 mmol) in dimethylformamide (40 ml) and the mixture stirred at ambient temperature for 4 hours. The mixture was filtered through Celite and then evaporated under reduced pressure. The residue was stirred in water (100 ml) for 30 minutes and then filtered and washed with water (25 ml) and then dried to leave 7-hydroxy-5-isopropoxyquinazolin-4(3H)-one (3.3 g, 100% yield) as a white solid:

후처리

  1. filtrationThe mixture was filtered through Celite
  2. customevaporated under reduced pressure
  3. stirringThe residue was stirred in water (100 ml) for 30 minutes
  4. filtrationfiltered
  5. washwashed with water (25 ml)
  6. customdried

출처 및 근거

ORD 기록
ord-a45ee6397e5249c299aca46e86a42b36
출처 데이터셋
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07691867B2

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