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Tert-butyl 2-cyano-5-{4-{(ethylsulfonyl)amino]phenyl}-1H-pyrrole-1-carboxylate → N-[4-(5-Cyano-1H-pyrrol-2-yl)phenyl]ethanesulfonamide

HRID 1591838
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HRID 1591838 반응식
C(OC([N:8]1[C:12]([C:13]2[CH:18]=[CH:17][C:16]([NH:19][S:20]([CH2:23][CH3:24])(=[O:22])=[O:21])=[CH:15][CH:14]=2)=[CH:11][CH:10]=[C:9]1[C:25]#[N:26])=O)(C)(C)C>CC(N(C)C)=O>[C:25]([C:9]1[NH:8][C:12]([C:13]2[CH:14]=[CH:15][C:16]([NH:19][S:20]([CH2:23][CH3:24])(=[O:22])=[O:21])=[CH:17][CH:18]=2)=[CH:11][CH:10]=1)#[N:26]
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참가 물질

3

반응물 1

HCID 16051190Tert-butyl 2-cyano-5-{4-{(ethylsulfonyl)amino]phenyl}-1H-pyrrole-1-carboxylate

생성물 1

HCID 16051191N-[4-(5-Cyano-1H-pyrrol-2-yl)phenyl]ethanesulfonamide수율 90%

시약·촉매·용매 1

HCID 31374Dimethylacetamide용매

반응 조건

온도
170 °C

실험 절차

Tert-butyl-2-cyano-5-{4-{(ethylsulfonyl)amino]phenyl}-1H-pyrrole-1-carboxylate (2.3 g, 6.1 mmol) was dissolved in dimethylacetamide (60 mL) and heated to 170° C. for 30 minutes. The mixture was cooled and partitioned between water and ethyl acetate. The organic layers were dried over magnesium sulfate, and concentrated. The residue was purified by silica gel Flash Chromatography (hexane/ethyl acetate; 1:1) to afford the title compound (1.51 g, 90%).

후처리

  1. temperatureThe mixture was cooled
  2. custompartitioned between water and ethyl acetate
  3. dry with materialThe organic layers were dried over magnesium sulfate
  4. concentrationconcentrated
  5. customThe residue was purified by silica gel Flash Chromatography (hexane/ethyl acetate; 1:1)

출처 및 근거

ORD 기록
ord-a4fb00caf82848528b29c9969102c477
출처 데이터셋
uspto-grants-2007_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07291643B2

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