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

HRID 639981
ノート
印刷プレビュー

反応式

HRID 639981 の反応式
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
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 6228Dimethylformamide溶媒

実験手順

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:

後処理

  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

出典と根拠

ORDレコード
ord-a45ee6397e5249c299aca46e86a42b36
出典データセット
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07691867B2

反応ノート

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