Formaldehyde → 4-Dimethylamino-6-methoxy-2-(4-tolylsulfonyl)methylamino-1,3,5-triazine

HRID 2165739Notes

Reaction equation

HRID 2165739 reaction equation
[NH2:1][C:2]1[N:7]=[C:6]([N:8]([CH3:10])[CH3:9])[N:5]=[C:4]([O:11][CH3:12])[N:3]=1.[C:13]1([CH3:22])[CH:18]=[CH:17][C:16]([S:19]([OH:21])=[O:20])=[CH:15][CH:14]=1.[Na].[CH3:24]S(O)(=O)=O.C=O>CO.O>[CH3:10][N:8]([CH3:9])[C:6]1[N:5]=[C:4]([O:11][CH3:12])[N:3]=[C:2]([NH:1][CH2:24][S:19]([C:16]2[CH:17]=[CH:18][C:13]([CH3:22])=[CH:14][CH:15]=2)(=[O:21])=[O:20])[N:7]=1

Participants

8

Reactant 5

HCID 712FormaldehydeHCID 6395Methanesulfonic AcidHCID 10818p-Toluenesulfinic acidHCID 7932556-Methoxy-N2,N2-dimethyl-1,3,5-triazine-2,4-diamineHCID 5360545Sodium

Product 1

HCID 230432274-Dimethylamino-6-methoxy-2-(4-tolylsulfonyl)methylamino-1,3,5-triazine

Reagents, catalysts & solvents 2

HCID 887MethanolSolventHCID 962WaterSolvent

Procedure

8.5 g (0.05 mole) of 2-amino-4-dimethylamino-6-methoxy-1,3,5-triazine and 9.1 g (0.05 mole) of toluene-4-sulfinic acid, sodium salt, are suspended in 100 ml of methanol and to the stirred suspension are added, in succession, 4.8 g (0.05 mole) of methanesulfonic acid and 4.7 g (0.055 mole) of aqueous 35% formaldehyde. The batch is then stirred for 30 minutes at room temperature and then for another 90 minutes under reflux. After cooling, the mixture is diluted with 1 liter of water and the crystalline precipitate is filtered with suction and dried. Melting point: 188°-190° C. Yield: 10 g (59% of theory).

Workup

  1. temperaturefor another 90 minutes under reflux
  2. temperatureAfter cooling
  3. filtrationthe crystalline precipitate is filtered with suction
  4. customdried

Sources & evidence

ORD record
ord-5e7054abbb0b44e6a43aa529306ee3df
Source dataset
uspto-grants-1990_07
Patent number
US04940792

Reaction notes

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