Methylamine → 5-Methylsulfamoyl-2-trifluoromethoxy-benzoic acid

HRID 1820721노트

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HRID 1820721 반응식
Cl[S:2]([C:5]1[CH:6]=[CH:7][C:8]([O:14][C:15]([F:18])([F:17])[F:16])=[C:9]([CH:13]=1)[C:10]([OH:12])=[O:11])(=[O:4])=[O:3].[CH3:19][NH2:20]>ClCCl.CO>[CH3:19][NH:20][S:2]([C:5]1[CH:6]=[CH:7][C:8]([O:14][C:15]([F:18])([F:17])[F:16])=[C:9]([CH:13]=1)[C:10]([OH:12])=[O:11])(=[O:4])=[O:3]

참가 물질

5

실험 절차

To a solution of 5-Chlorosulfonyl-2-trifluoromethoxy-benzoic acid (0.15 g) in dichloromethane (1.5 ml) was added a solution of methylamine in methanol (8M, 0.31 mL), and the reaction mixture was stirred for 2 minutes after precipitation was complete. The reaction mixture was then concentrated in vacuo and the residue was dissolved in 1N NaOH (2 mL) and extracted with diethylether. The aqueous phase was then acidified using 3 N hydrochloric acid solution (2 mL), and the solution was extracted with dichloromethane (2×10 mL). The combined organic phases were dried with sodium sulfate and concentrated in vacuo to yield the title compound as a white solid (0.12 g). MS (m/e): 298.0 (M−H, 100%).

후처리

  1. customafter precipitation
  2. concentrationThe reaction mixture was then concentrated in vacuo
  3. dissolutionthe residue was dissolved in 1N NaOH (2 mL)
  4. extractionextracted with diethylether
  5. extractionthe solution was extracted with dichloromethane (2×10 mL)
  6. dry with materialThe combined organic phases were dried with sodium sulfate
  7. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-ba6b1ebf4b104ac381dfa98fdd99a149
출처 데이터셋
uspto-grants-2009_10
특허 번호
US07605163B2

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