3,5-Dimethylpyridine → Penoxsulam

HRID 1391845Notes

Reaction equation

HRID 1391845 reaction equation
[NH2:1][C:2]1[N:10]=[C:9]2[N:4]([C:5]([O:13][CH3:14])=[N:6][CH:7]=[C:8]2[O:11][CH3:12])[N:3]=1.[F:15][CH:16]([F:33])[CH2:17][O:18][C:19]1[CH:24]=[CH:23][CH:22]=[C:21]([C:25]([F:28])([F:27])[F:26])[C:20]=1[S:29](Cl)(=[O:31])=[O:30].N1C=C(C)C=C(C)C=1>CS(C)=O>[F:33][CH:16]([F:15])[CH2:17][O:18][C:19]1[CH:24]=[CH:23][CH:22]=[C:21]([C:25]([F:26])([F:27])[F:28])[C:20]=1[S:29]([NH:1][C:2]1[N:10]=[C:9]2[N:4]([C:5]([O:13][CH3:14])=[N:6][CH:7]=[C:8]2[O:11][CH3:12])[N:3]=1)(=[O:30])=[O:31]

Participants

5

Reactant 3

HCID 115653,5-DimethylpyridineHCID 114468885,8-Dimethoxy-[1,2,4]triazolo[1,5-c]pyrimidin-2-amineHCID 160503082-(2,2-Difluoroethoxy)-6-(trifluoromethyl)benzene-1-sulfonyl chloride

Product 1

HCID 11784975PenoxsulamYield 93.1%

Reagents, catalysts & solvents 1

HCID 679Dimethyl SulfoxideCatalyst

Procedure

2-Amino-5,8-dimethoxy[1,2,4]triazolo[1,5-c]pyrimidine (7.8 g, 0.040 mol) and 2-(2,2-difluoroethoxy)-6-(trifluoromethyl)benzenesulfonyl chloride (13 g, 0.040 mol) were combined in 3,5-lutidine (31 g, 0.29 mol, 7.2 eq). The slurry was treated with methyl sulfoxide (0.040 g, 0.0005 mol, 0.012 eq) and stirred at ambient conditions for 8.5 hours. The reaction slurry was filtered, and the wet cake solids were slurried in a mixture of 15% sulfuric acid (80 mL) and acetonitrile (20 mL). The mixture was stirred for 25 minutes, then filtered, and the solids washed with water. After drying under vacuum at 55° C., 18 g of product was obtained as a white solid assaying at 97.4 wt % (91% yield).

Workup

  1. filtrationThe reaction slurry was filtered
  2. additionthe wet cake solids were slurried in a mixture of 15% sulfuric acid (80 mL) and acetonitrile (20 mL)
  3. stirringThe mixture was stirred for 25 minutes
  4. filtrationfiltered
  5. washthe solids washed with water
  6. customAfter drying under vacuum at 55° C.

Sources & evidence

ORD record
ord-a80a7b96a6d543f8a45591549157c42c
Source dataset
uspto-grants-2008_03
Patent number
US07339058B2

Reaction notes

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