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Chlorosulfamic acid → 2-Sulfamoylaminocyclopent-1-enecarbonitrile

HRID 471573
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HRID 471573 반응식
[NH2:1][C:2]1[CH2:6][CH2:5][CH2:4][C:3]=1[C:7]#[N:8].[S:9](Cl)(=[O:12])(=[O:11])[NH2:10]>CC(N(C)C)=O.CCOC(C)=O>[S:9]([NH:1][C:2]1[CH2:6][CH2:5][CH2:4][C:3]=1[C:7]#[N:8])(=[O:12])(=[O:11])[NH2:10]
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참가 물질

5

반응물 2

HCID 24499Chlorosulfamic acidHCID 2872752-Amino-1-cyclopentene-1-carbonitrile

생성물 1

HCID 673976352-Sulfamoylaminocyclopent-1-enecarbonitrile

시약·촉매·용매 2

HCID 8857Ethyl Acetate용매HCID 31374Dimethylacetamide용매

실험 절차

To a solution of 2-aminocyclopent-1-enecarbonitrile (440 mg, 4.07 mmol) in 10 mL of DMA was added sulfamoyl chloride (941.3 mg, 8.15 mmol), and the resultant mixture was stirred at room temperature under nitrogen for 2 h. Then it was diluted with EtOAc, the organic layer was washed with brine and dried down under vacuum, and the residue was purified by chromatography on silica gel eluting with EtOAc/Hexane to give the title compound. 1H NMR (400 MHz, CDCl3) δ 2.04-1.97 (m, 2H), 2.61-2.57 (m, 2H), 2.9-2.86 (m, 2H), 5.66 (s, 2H), 8.04 (s, 1H).

후처리

  1. washthe organic layer was washed with brine
  2. customdried down under vacuum
  3. customthe residue was purified by chromatography on silica gel eluting with EtOAc/Hexane

출처 및 근거

ORD 기록
ord-34dcd856750a48a5bf6c9d021b341f9b
출처 데이터셋
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08633186B2

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