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Ammonia → 7-(benzyloxy)-5-isopropoxyquinazolin-4(3H)-one

HRID 639980
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HRID 639980 반응식
C(OC[N:9]1[C:18](=[O:19])[C:17]2[C:12](=[CH:13][C:14]([O:24][CH2:25][C:26]3[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=3)=[CH:15][C:16]=2[O:20][CH:21]([CH3:23])[CH3:22])[N:11]=[CH:10]1)(=O)C(C)(C)C.N>CO>[CH2:25]([O:24][C:14]1[CH:13]=[C:12]2[C:17]([C:18](=[O:19])[NH:9][CH:10]=[N:11]2)=[C:16]([O:20][CH:21]([CH3:23])[CH3:22])[CH:15]=1)[C:26]1[CH:27]=[CH:28][CH:29]=[CH:30][CH:31]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 222AmmoniaHCID 68639837[7-(benzyloxy)-5-isopropoxy-4-oxoquinazolin-3(4H)-yl]methyl pivalate

생성물 1

HCID 1355106847-(benzyloxy)-5-isopropoxyquinazolin-4(3H)-one수율 87%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

[7-(benzyloxy)-5-isopropoxy-4-oxoquinazolin-3(4H)-yl]methyl pivalate was stirred in a 7N solution of ammonia in methanol (250 ml) at room temperature for 24 hours. The mixture was evaporated under reduced pressure and the residue purified by silica gel chromatography eluting with a 0 to 10% mixture of methanol in dichloromethane to give 7-(benzyloxy)-5-isopropoxyquinazolin-4(3H)-one (4.6 g, 87% yield over 2 steps) as a white solid:

후처리

  1. customThe mixture was evaporated under reduced pressure
  2. customthe residue purified by silica gel chromatography
  3. washeluting with a 0 to 10% mixture of methanol in dichloromethane

출처 및 근거

ORD 기록
ord-b298554e27ff44a18dada374b7f913bd
출처 데이터셋
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07691867B2

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