Hydrochloric Acid → 3-Anilino-4-acetyl-5-methylpyrazole

HRID 1447194Notes

Reaction equation

HRID 1447194 reaction equation
[C:1]1([NH:7][C:8](=S)[NH:9][NH2:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Cl.Cl[CH2:14][C:15]([CH2:17][C:18](=O)[CH3:19])=[O:16]>O1CCCC1>[NH:7]([C:8]1[C:17]([C:15](=[O:16])[CH3:14])=[C:18]([CH3:19])[NH:10][N:9]=1)[C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

5

Reactant 3

HCID 313Hydrochloric AcidHCID 730679Hydrazinecarbothioamide, N-phenyl-HCID 144968561-Chloro-2,4-pentanedione

Product 1

HCID 204753773-Anilino-4-acetyl-5-methylpyrazole

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

50 g of 4-phenylthiosemicarbazide is suspended in 300 ml of tetrahydrofuran and 0.5 ml of concentrated HCl is added. Then 40.4 g of 3-chloroacetyl acetone is allowed to run in all at once and the whole is cooled with an ice-bath. After 12 hours' stirring, the precipitate formed is suction filtered, washed with acetone and then boiled in a water/acetone mixture (1:1). This hot solution is filtered off from the sulfur and neutralized with aqueous ammonia solution. The product is then suction filtered and recrystallized from acetone; m.p. 246°-247° C.

Workup

  1. temperatureis cooled with an ice-bath
  2. customthe precipitate formed
  3. filtrationfiltered
  4. washwashed with acetone
  5. filtrationThis hot solution is filtered off from the sulfur and neutralized with aqueous ammonia solution
  6. filtrationsuction filtered
  7. customrecrystallized from acetone

Sources & evidence

ORD record
ord-0157f38d15164dd29197e02c16ab6b2d
Source dataset
uspto-grants-1982_02
Patent number
US04316039

Reaction notes

Loading…