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4-Bromophenacyl bromide → 2-Amino-5-(4-bromophenyl)pyrrole-3-carboxamide

HRID 1011565
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HRID 1011565 반응식
[O-]CC.[Na+].[CH2:5]([C:9]([NH2:11])=[O:10])[C:6]([NH2:8])=[NH:7].Cl.Br[CH2:14][C:15]([C:17]1[CH:22]=[CH:21][C:20]([Br:23])=[CH:19][CH:18]=1)=O>C(O)C>[NH2:7][C:6]1[NH:8][C:15]([C:17]2[CH:22]=[CH:21][C:20]([Br:23])=[CH:19][CH:18]=2)=[CH:14][C:5]=1[C:9]([NH2:11])=[O:10]
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참가 물질

5

반응물 3

HCID 74544-Bromophenacyl bromideHCID 2723922Sodium ethoxideHCID 3084595Amidinomalonamide hydrochloride

생성물 1

HCID 592859782-Amino-5-(4-bromophenyl)pyrrole-3-carboxamide수율 9%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Under ice-cooling, sodium ethoxide (2.1 g, 30 mmol) was added to a suspension of malonamamidine hydrochloride (4.1 g, 30 mmol) in dehydrated ethanol (50 mL), and then the mixture was stirred for 20 minutes. Moreover, 2,4′-dibromoacetophenone (4.2 g, 15 mmol) was added thereto, and the whole was stirred at room temperature for 5 hours. After the insoluble solid was filtered out, the filtrate was concentrated in vacuo. The obtained residue was purified by silica gel column chromatography to give the title reference compound (0.37 g) as a black solid (Yield 9%).

후처리

  1. temperatureUnder ice-cooling
  2. stirringthe whole was stirred at room temperature for 5 hours
  3. filtrationAfter the insoluble solid was filtered out
  4. concentrationthe filtrate was concentrated in vacuo
  5. customThe obtained residue was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-b2436f09308e4ebf8d1fc7d84b09038e
출처 데이터셋
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07977371B2

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