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Ammonia → 2-Aminocarbonylamino-5-(4-bromophenyl)pyrrole-3-carboxamide

HRID 1011571
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HRID 1011571 반응식
ClC(Cl)(Cl)[C:3]([N:5]=C=O)=[O:4].[NH2:10][C:11]1[NH:12][C:13]([C:19]2[CH:24]=[CH:23][C:22]([Br:25])=[CH:21][CH:20]=2)=[CH:14][C:15]=1[C:16]([NH2:18])=[O:17].N.CO>O1CCCC1.O>[NH2:5][C:3]([NH:10][C:11]1[NH:12][C:13]([C:19]2[CH:24]=[CH:23][C:22]([Br:25])=[CH:21][CH:20]=2)=[CH:14][C:15]=1[C:16]([NH2:18])=[O:17])=[O:4]
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참가 물질

7

반응물 4

HCID 222AmmoniaHCID 887MethanolHCID 76400Trichloroacetyl isocyanateHCID 592859782-Amino-5-(4-bromophenyl)pyrrole-3-carboxamide

생성물 1

HCID 250057042-Aminocarbonylamino-5-(4-bromophenyl)pyrrole-3-carboxamide수율 36%

시약·촉매·용매 2

HCID 962Water
용매
HCID 8028Tetrahydrofuran용매

실험 절차

Trichloroacetyl isocyanate (60 μL, 0.50 mmol) was added dropwise to a solution of 2-amino-5-(4-bromophenyl)pyrrole-3-carboxamide (Reference compound No. 1-1, 0.17 g, 0.60 mmol) in anhydrous tetrahydrofuran (3.0 mL) at −40° C. and the mixture was stirred for 1 hour. Furthermore, ammonia solution 2.0 M in methanol (3.0 mL, 6.0 mmol) was added thereto, and the whole was stirred at room temperature for 3 days. Water (20 mL) was added to the reaction solution, then the precipitated solid was filtered off. The obtained solid was dried under reduced pressure to give the target compound (0.070 g) as a brown solid (Yield 36%).

후처리

  1. filtrationthe precipitated solid was filtered off
  2. customThe obtained solid was dried under reduced pressure

출처 및 근거

ORD 기록
ord-1c7be30331e74cf3ab4d22d2ee4f973f
출처 데이터셋
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07977371B2

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