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Methanol → HCID 19791270, 화합물

HRID 1655196
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HRID 1655196 반응식
Cl.Cl.[C:3]([N:6]1[CH2:11][CH2:10][N:9]([NH2:12])[CH2:8][CH2:7]1)(=[O:5])[CH3:4].C(N(CC)CC)C.[F:20][C:21]1[CH:26]=[CH:25][C:24]([N:27]=[C:28]=[O:29])=[CH:23][CH:22]=1.CO>ClCCl>[C:3]([N:6]1[CH2:11][CH2:10][N:9]([NH:12][C:28]([NH:27][C:24]2[CH:25]=[CH:26][C:21]([F:20])=[CH:22][CH:23]=2)=[O:29])[CH2:8][CH2:7]1)(=[O:5])[CH3:4]
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참가 물질

6

반응물 4

HCID 887MethanolHCID 8471TriethylamineHCID 709554-Fluorophenyl isocyanateHCID 21701657HCID 21701657, 화합물

생성물 1

HCID 19791270HCID 19791270, 화합물수율 71.4%

시약·촉매·용매 1

HCID 6344Dichloromethane용매3회

실험 절차

To a solution of 1-acetyl-4-aminopiperazine dihydrochloride (540 mg) in dichloromethane (5 ml) was added dropwise triethylamine (0.8 ml) followed by addition a solution of 4-fluorophenylisocyanate (377 mg) in dichloromethane (2.5 ml) with stirring in an ice bath. After stirring for 100 minutes at the same temperature, a mixture of dichloromethane (15 ml) and methanol (3 ml) was added to the reaction mixture. The mixture was washed with brine, dried, and concentrated in vacuo. The residue was crystallized from ethanol to yield N-(4-acetyl-1-piperazinyl)-N'-(4-fluoroph-enyl)urea (500 mg).

후처리

  1. stirringAfter stirring for 100 minutes at the same temperature
  2. additionwas added to the reaction mixture
  3. washThe mixture was washed with brine
  4. customdried
  5. concentrationconcentrated in vacuo
  6. customThe residue was crystallized from ethanol

출처 및 근거

ORD 기록
ord-a8ec0385cd77455a8699198d80df9991
출처 데이터셋
uspto-grants-1993_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05250528

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