Dimethyl Sulfoxide → N-(4-Bromo-1-methylpyrazol-3-yl)-7-chloro-5-methoxy-1,2,4-triazolo[1,5-c]-pyrimidine-2-sulfonamide

HRID 1589998노트

반응식

HRID 1589998 반응식
N1C=CC=CC=1.CS(C)=O.[Cl:11][C:12]1[N:17]=[C:16]([O:18][CH3:19])[N:15]2[N:20]=[C:21]([S:23](Cl)(=[O:25])=[O:24])[N:22]=[C:14]2[CH:13]=1.[NH2:27][C:28]1[C:32]([Br:33])=[CH:31][N:30]([CH3:34])[N:29]=1>C(#N)C>[Br:33][C:32]1[C:28]([NH:27][S:23]([C:21]2[N:22]=[C:14]3[N:15]([C:16]([O:18][CH3:19])=[N:17][C:12]([Cl:11])=[CH:13]3)[N:20]=2)(=[O:25])=[O:24])=[N:29][N:30]([CH3:34])[CH:31]=1

참가 물질

6

반응물 4

HCID 679Dimethyl SulfoxideHCID 1049PyridineHCID 27352834-bromo-1-methyl-1H-pyrazol-3-amineHCID 150036517-Chloro-5-methoxy-1,2,4-triazolo[1,5-c]pyrimidine-2-sulfonyl chloride

생성물 1

HCID 19768914N-(4-Bromo-1-methylpyrazol-3-yl)-7-chloro-5-methoxy-1,2,4-triazolo[1,5-c]-pyrimidine-2-sulfonamide

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

Pyridine (1.08 g, 8.0 mmol) and dimethyl sulfoxide (0.2 g) were added to a solution of 7-chloro-5-methoxy-1,2,4-triazolo[1,5-c]pyrimidine-2-sulfonyl chloride (1.0 g, 4.0 mmol) and 3-amino-4-bromo-1-methylpyrazole (0.70 g, 4.0 mmol) in 10 mL of acetonitrile with stirring at ambient temperature and the mixture was allowed to react overnight. The mixture was then concentrated by evaporation under reduced pressure and the residue was taken up in methylene chloride. The resulting solution was extracted with water and dried over magnesium sulfate. The volatile materials were then removed by evaporation under reduced pressure and the solid residue was extracted with diethyl ether and with water, recovered by filtration, and dried under reduced pressure to obtain 0.38 g (25 percent of theory) of the title compound as a white solid melting at 230°-232° C.

후처리

  1. customto react overnight
  2. concentrationThe mixture was then concentrated by evaporation under reduced pressure
  3. extractionThe resulting solution was extracted with water
  4. dry with materialdried over magnesium sulfate
  5. customThe volatile materials were then removed by evaporation under reduced pressure
  6. extractionthe solid residue was extracted with diethyl ether and with water
  7. filtrationrecovered by filtration
  8. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-ba3653cb416548de924fafa6dbeb8b7c
출처 데이터셋
uspto-grants-1993_04
특허 번호
US05201938

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