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Formamidine acetate → 7-Benzyloxy-6-methoxy-3H-quinazolin-4-one

HRID 538905
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HRID 538905 반응식
[NH2:1][C:2]1[CH:17]=[C:16]([O:18][CH2:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[C:15]([O:26][CH3:27])=[CH:14][C:3]=1[C:4](OCC1C=CC=CC=1)=[O:5].C(O)(=O)C.[CH:32](N)=[NH:33]>C(O)C(C)C>[CH2:19]([O:18][C:16]1[CH:17]=[C:2]2[C:3]([C:4](=[O:5])[NH:33][CH:32]=[N:1]2)=[CH:14][C:15]=1[O:26][CH3:27])[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 160693Formamidine acetateHCID 11057568Benzyl 2-amino-4-(benzyloxy)-5-methoxybenzoate

생성물 1

HCID 1354047187-Benzyloxy-6-methoxy-3H-quinazolin-4-one

시약·촉매·용매 1

HCID 6560Isobutanol용매

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온도
97 °C

실험 절차

Benzyl 2-amino-4-(benzyloxy)-5-methoxybenzoate (80.0 g), formamidine acetate (32.0 g) and isobutanol (480 ml) were mixed. The reaction mixture was then heated to 97° C. and stirred at this temperature for 6 hours. The reaction mixture was then cooled to 25° C. over a period of at least an hour and then stirred at this temperature for 30 minutes. The product (7-benzyloxy-6-methoxy-3,4-dihydroquinazolin-4-one) was isolated by filtration, washed with isobutanol (64.2 g) and dried in the vacuum oven at a temperature of from 40 to 45° C. Yield: 60.8 g, 98%; NMR Spectrum (DMSOd6) 3.9 (s, 3H), 5.3 (s, 2H), 7.3 (s, 1H), 7.3-7.5 (m, 6H), 8.0 (s, 1H); Mass Spectrum (M+H)+=283.1.

후처리

  1. temperatureThe reaction mixture was then cooled to 25° C. over a period of at least an hour
  2. stirringstirred at this temperature for 30 minutes

출처 및 근거

ORD 기록
ord-85093ba7d799469db7885e04d5090313
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08865899B2

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