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Sulfamide → 2-Sulfamoylamino-6-(3-(trimethylsilyl)prop-1-ynyl)benzonitrile

HRID 471752
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HRID 471752 반응식
[NH2:1][C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([C:10]#[C:11][CH2:12][Si:13]([CH3:16])([CH3:15])[CH3:14])[C:3]=1[C:4]#[N:5].[NH2:17][S:18](N)(=[O:20])=[O:19]>O1CCOCC1>[S:18]([NH:1][C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([C:10]#[C:11][CH2:12][Si:13]([CH3:14])([CH3:16])[CH3:15])[C:3]=1[C:4]#[N:5])(=[O:20])(=[O:19])[NH2:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 82267SulfamideHCID 674002162-Amino-6-(3-(trimethylsilyl)prop-1-ynyl)benzonitrile

생성물 1

HCID 674011982-Sulfamoylamino-6-(3-(trimethylsilyl)prop-1-ynyl)benzonitrile수율 5%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

A solution of 2-amino-6-(3-(trimethylsilyl)prop-1-ynyl)benzonitrile (Example 253b) (557 mg, 2.0 mmol) and NH2SO2NH2 (0.96 g, 10 mmol) in dry 1,4-dioxane (50 mL) was refluxed under nitrogen for 2 days. The solvent was evaporated under reduced pressure, and the residue was purified by chromatography on silica gel eluting with 70% EtOAc in hexanes to give the title compound (31 mg, 5%) as a white solid. MS 308 (MH+).

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후처리

  1. customThe solvent was evaporated under reduced pressure
  2. customthe residue was purified by chromatography on silica gel eluting with 70% EtOAc in hexanes

출처 및 근거

ORD 기록
ord-c60470cedb024c8f80a43eafc2d41869
출처 데이터셋
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08633186B2

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