Sodium Bicarbonate → 5-amino-1-[2,6-dichloro4-(trifluoromethyl)phenyl]-3-[(1,1-dimethoxy)ethyl]4-methylthio-1H-pyrazole

HRID 1937447Notes

Reaction equation

HRID 1937447 reaction equation
[C:1]([C:4]1[C:8]([S:9][CH3:10])=[C:7]([NH2:11])[N:6]([C:12]2[C:17]([Cl:18])=[CH:16][C:15]([C:19]([F:22])([F:21])[F:20])=[CH:14][C:13]=2[Cl:23])[N:5]=1)(=[O:3])[CH3:2].[CH:24]([O-:27])([O-])[O-].O.[C:29]1(C)C=CC(S(O)(=O)=O)=CC=1.C([O-])(O)=O.[Na+]>CO>[NH2:11][C:7]1[N:6]([C:12]2[C:17]([Cl:18])=[CH:16][C:15]([C:19]([F:20])([F:21])[F:22])=[CH:14][C:13]=2[Cl:23])[N:5]=[C:4]([C:1]([O:27][CH3:24])([O:3][CH3:29])[CH3:2])[C:8]=1[S:9][CH3:10]

Participants

6

Conditions

Temperature
40 °C

Procedure

A mixture of 2.0 g (0.0052 mole) of 3-acetyl-5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-methylthio-1H-pyrazole, 1.7 ml (0.0156 mole) of trinethyl orthoformate, 0.060 g (0.0003 mole) of para-toluenesulfonic acid monohydrate and 10 ml of methanol was heated at 40° C. for about 8 hours, then left 64 h at 20° C. The mixture was mixed with a saturated solution of NaHCO3, extracted with dichloromethane, and successively dried, filtered, evaporated, chromatographed on silica gel. 0.59 g of the title compound having a melting point of about 149° C. was obtained.

Workup

  1. extractionextracted with dichloromethane
  2. customsuccessively dried
  3. filtrationfiltered
  4. customevaporated
  5. customchromatographed on silica gel
  6. customwas obtained

Sources & evidence

ORD record
ord-2ff09b5381de4107b485e13b8b5a6287
Source dataset
uspto-grants-2002_05
Patent number
US06395760B1

Reaction notes

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