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Ammonia → 4-(alpha-Carbamoyl-3,4-methylenedioxybenzyl)amino-6-chloroquinazoline

HRID 1003516
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인쇄 미리보기

반응식

HRID 1003516 반응식
[NH3:1].C([O:4][C:5]([CH:7]([NH:17][C:18]1[C:27]2[C:22](=[CH:23][CH:24]=[C:25]([Cl:28])[CH:26]=2)[N:21]=[CH:20][N:19]=1)[C:8]1[CH:13]=[CH:12][C:11]2[O:14][CH2:15][O:16][C:10]=2[CH:9]=1)=O)C>C(O)C>[C:5]([CH:7]([NH:17][C:18]1[C:27]2[C:22](=[CH:23][CH:24]=[C:25]([Cl:28])[CH:26]=2)[N:21]=[CH:20][N:19]=1)[C:8]1[CH:13]=[CH:12][C:11]2[O:14][CH2:15][O:16][C:10]=2[CH:9]=1)(=[O:4])[NH2:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 222AmmoniaHCID 18796707HCID 18796707, 화합물

생성물 1

HCID 187967044-(alpha-Carbamoyl-3,4-methylenedioxybenzyl)amino-6-chloroquinazoline수율 32%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

20 ml of a 10% solution of ammonia in ethanol was added to 200 mg of 4-(α-ethoxycarbonyl-3,4-methylenedioxybenzyl)amino-6-chloroquinazoline. The obtained mixture was stirred at room temperature for 3 days. The crystal thus precipitated was recovered by filtration. Thus, 60 mg of the title compounds was obtained.

후처리

  1. customThe crystal thus precipitated
  2. filtrationwas recovered by filtration

출처 및 근거

ORD 기록
ord-92bd9c5a35c64d60b0ab51cec071d491
출처 데이터셋
uspto-grants-2000_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06046206

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