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Thionyl Chloride → Isoquinoline-5-sulfonyl chloride hydrochloride

HRID 2118497
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HRID 2118497 반응식
[CH:1]1[C:10]2[CH:9]=[CH:8][CH:7]=[C:6]([S:11]([OH:14])(=O)=[O:12])[C:5]=2[CH:4]=[CH:3][N:2]=1.S(Cl)([Cl:17])=O>>[ClH:17].[CH:1]1[C:10]2[CH:9]=[CH:8][CH:7]=[C:6]([S:11]([Cl:17])(=[O:14])=[O:12])[C:5]=2[CH:4]=[CH:3][N:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24386Thionyl ChlorideHCID 2415995-Isoquinolinesulfonic acid

생성물 1

HCID 13116932Isoquinoline-5-sulfonyl chloride hydrochloride

실험 절차

To 1200 ml of thionyl chloride were added 150 g of 5-isoquinolinesulfonic acid and 0.4 ml of N,Ndimethylformamide. Then, the resulting mixture was refluxed while heating at 80° to 85 ° C for 3 hours, followed by removal of the thionyl chloride under reduced pressure. Subsequently, 300 ml of dichloromethane was added to the reaction mixture to precipitate crystals. The precipitated crystals were separated by filtration, washed with 100 ml of dichloromethane, and then dried under reduced pressure to obtain 170 g of 5-isoquinolinesulfonyl chloride hydrochloride.

후처리

  1. temperatureThen, the resulting mixture was refluxed
  2. temperaturewhile heating at 80° to 85 ° C for 3 hours
  3. customfollowed by removal of the thionyl chloride under reduced pressure
  4. addition
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
Subsequently, 300 ml of dichloromethane was added to the reaction mixture
  • customto precipitate crystals
  • customThe precipitated crystals were separated by filtration
  • washwashed with 100 ml of dichloromethane
  • customdried under reduced pressure
  • 출처 및 근거

    ORD 기록
    ord-1c9cce957c6541c6bad7e27fdb0e10ea
    출처 데이터셋
    uspto-grants-1987_07
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04678783

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