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Diisopropylcarbodiimide → HCID 46871734, 화합물

HRID 1410194
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인쇄 미리보기

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HRID 1410194 반응식
CC(N=C=NC(C)C)C.[C:10]([NH:13][CH:14]([C:16]1[CH:17]=[CH:18][C:19]([Cl:44])=[C:20]([NH:22][C:23](=S)[NH:24][C:25]2[CH:26]=[C:27]([CH:38]=[CH:39][C:40]=2[NH:41][CH3:42])[C:28]([NH:30][C:31]2[CH:36]=[CH:35][C:34]([Br:37])=[CH:33][CH:32]=2)=[O:29])[CH:21]=1)[CH3:15])(=[O:12])[CH3:11]>CN(C=O)C>[C:10]([NH:13][CH:14]([C:16]1[CH:17]=[CH:18][C:19]([Cl:44])=[C:20]([NH:22][C:23]2[N:41]([CH3:42])[C:40]3[CH:39]=[CH:38][C:27]([C:28]([NH:30][C:31]4[CH:36]=[CH:35][C:34]([Br:37])=[CH:33][CH:32]=4)=[O:29])=[CH:26][C:25]=3[N:24]=2)[CH:21]=1)[CH3:15])(=[O:12])[CH3:11]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 12734DiisopropylcarbodiimideHCID 59529808HCID 59529808, 화합물

생성물 1

HCID 46871734HCID 46871734, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
80 °C

실험 절차

N,N-Diisopropylcarbodiimide (46 L, 0.2 mmol) was added to 3-{3-[5-(1-acet-amidoethyl)-2-chlorophenyl]thioureido}-N-(4-bromophenyl)-4-(methylamino)benzamide (130 mg, 0.2 mmol) in DMF (2 mL) at rt. The mixture was stirred at 80° C. for 2 h, cooled and concentrated. The residue was purified by chromatography to give the title compound.

후처리

  1. temperaturecooled
  2. concentrationconcentrated
  3. customThe residue was purified by chromatography

출처 및 근거

ORD 기록
ord-701004dd933c4966be15f6e77b633e91
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08921405B2

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