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2-(3',4'-Diamino-biphenyl-2-sulfonyl)-ethanol → HCID 178504704, 화합물

HRID 1433228
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인쇄 미리보기

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HRID 1433228 반응식
[NH2:1][C:2]1[CH:3]=[C:4]([C:9]2[C:10]([S:15]([CH2:18]CO)(=[O:17])=[O:16])=[CH:11][CH:12]=[CH:13][CH:14]=2)[CH:5]=[CH:6][C:7]=1[NH2:8].Cl.C(O[C:25](=N)[CH2:26][Br:27])C>C(O)C>[Br:27][CH2:26][C:25]1[NH:8][C:7]2[CH:6]=[CH:5][C:4]([C:9]3[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=3[S:15]([CH3:18])(=[O:16])=[O:17])=[CH:3][C:2]=2[N:1]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 579349382-(3',4'-Diamino-biphenyl-2-sulfonyl)-ethanolHCID 75357914Ethyl 2-bromoethanecarboximidate hydrochloride

생성물 1

HCID 178504704HCID 178504704, 화합물수율 101.7%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of 2-(3′,4′-diamino-biphenyl-2-sulfonyl)-ethanol (0.140 g, 0.479 mmol) and 2-bromoacetimidic acid ethyl ester hydrochloride salt (0.116 g, 0.575 mmol) in anhydrous ethanol (100%, 6 mL) was stirred at room temperature for 12 hours. The reaction mixture was concentrated under reduced pressure and extracted with ethyl acetate and brine. The organic layer was dried over Na2SO4, filtered, and the filtrate was concentrated in vacuo to provide 2-bromomethyl-5-(2-methanesulfonyl-phenyl)-1H-benzoimidazole as yellow oil (0.178 g, 94%).

후처리

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. extractionextracted with ethyl acetate and brine
  3. dry with materialThe organic layer was dried over Na2SO4
  4. filtrationfiltered
  5. concentrationthe filtrate was concentrated in vacuo

출처 및 근거

ORD 기록
ord-1e8e12eb95b34590b901bf99812bdcc2
출처 데이터셋
uspto-grants-2009_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07612211B2

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