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

HRID 1645964ノート

反応式

HRID 1645964 の反応式
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

参加物

6

反応物 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

生成物 1

HCID 19768914N-(4-Bromo-1-methylpyrazol-3-yl)-7-chloro-5-methoxy-1,2,4-triazolo[1,5-c]-pyrimidine-2-sulfonamide収率 25%

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

Pyridine (1.08 g, 8 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 (0.7 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 MgSO4. 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 yield) of the title compound as a white solid melting at 230°-232° C.

後処理

  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 MgSO4
  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

出典と根拠

ORDレコード
ord-ec4798ddd9b9472680f8a946022a9d8d
出典データセット
uspto-grants-1993_01
特許番号
US05177206

反応ノート

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