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Ethanol → 4-(alpha-Carboxy-3,4-methylenedioxybenzyl)amino-6-chloroquinazoline

HRID 1003515
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HRID 1003515 반응식
C(O)C.[OH-].[Na+].C([O:8][C:9]([CH:11]([NH:21][C:22]1[C:31]2[C:26](=[CH:27][CH:28]=[C:29]([Cl:32])[CH:30]=2)[N:25]=[CH:24][N:23]=1)[C:12]1[CH:17]=[CH:16][C:15]2[O:18][CH2:19][O:20][C:14]=2[CH:13]=1)=[O:10])C>O>[C:9]([CH:11]([NH:21][C:22]1[C:31]2[C:26](=[CH:27][CH:28]=[C:29]([Cl:32])[CH:30]=2)[N:25]=[CH:24][N:23]=1)[C:12]1[CH:17]=[CH:16][C:15]2[O:18][CH2:19][O:20][C:14]=2[CH:13]=1)([OH:10])=[O:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 702EthanolHCID 14798Sodium HydroxideHCID 18796707HCID 18796707, 화합물

생성물 1

HCID 187966624-(alpha-Carboxy-3,4-methylenedioxybenzyl)amino-6-chloroquinazoline수율 49%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

10 ml of ethanol, 5 ml of water and 20 mg of sodium hydroxide were added to 100 mg of 4-(α-ethoxycarbonyl-3,4-methylenedioxybenzyl)amino-6-chloroquinazoline. The obtained mixture was refluxed for 10 minutes and concentrated under a reduced pressure, followed by the addition of 20 ml of water. The obtained mixture was neutralized with 1N hydrochloric acid. The crystal thus precipitated was recovered by filtration. Thus, 45 mg of the title compound was obtained.

후처리

  1. temperatureThe obtained mixture was refluxed for 10 minutes
  2. concentrationconcentrated under a reduced pressure
  3. additionfollowed by the addition of 20 ml of water
  4. customThe crystal thus precipitated
  5. filtrationwas recovered by filtration

출처 및 근거

ORD 기록
ord-83928056127541fa8c844ce6e531513b
출처 데이터셋
uspto-grants-2000_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06046206

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