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Triethylamine → HCID 178423399, 화합물

HRID 540297
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HRID 540297 반응식
Cl[C:2]1[NH:11][C:10](=[O:12])[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=1.[CH2:13]1[C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][C:18]=2[C:17](=[O:24])[CH2:16][CH2:15][NH:14]1.[CH2:25](N(CC)CC)C>C1(C)C=CC=CC=1>[OH:12][C:10]1[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([CH3:25])[CH:8]=2)[N:3]=[C:2]([N:14]2[CH2:15][CH2:16][C:17](=[O:24])[C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=3[CH2:13]2)[N:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 56924244HCID 56924244, 화합물HCID 1354432322-Chloroquinazolin-4(3H)-one

생성물 1

HCID 178423399HCID 178423399, 화합물수율 81%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

To a stirred solution of 2-chloro-4(3H)-quinazolinone (580 mg, 3.0 mmol) and 1,2,3,4-tetrahydro-5H-2-benzazepin-5-one (591 mg, 3.0 mmol) in toluene (20 mL) was added triethylamine (626 μL, 4.5 mmol). After being refluxed overnight, the resulting reaction mixture was cooled and the formed solid was collected by filtration, washed with ethanol (10 mL) and ethyl acetate (10 mL), and dried in vacuo to afford 775 mg of the desired product as a white solid (yield was 81%).

후처리

  1. temperatureAfter being refluxed overnight
  2. customthe resulting reaction mixture
  3. temperaturewas cooled
  4. filtrationthe formed solid was collected by filtration
  5. washwashed with ethanol (10 mL) and ethyl acetate (10 mL)
  6. customdried in vacuo

출처 및 근거

ORD 기록
ord-2eb8c850279048fc9345bbd9b64930c7
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08871756B2

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