Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460736Generated: October 29, 2026

Hydrochloric Acid → 1-(2,4,6-Trichlorophenyl)-2-acetyl-3-(2-chloro-5-myristoylaminoanilino)-3-pyrazolin-5-one

https://huagongshe.com/reaction/460736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetyl chlorideHCID 6367—
Reactant2,6-LutidineHCID 7937—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantN-[4-chloro-3-[[5-oxo-1-(2,4,6-trichlorophenyl)-4H-pyrazol-3-yl]amino]phenyl]tetradecanamideHCID 178443172—
SolventDichloromethaneHCID 6344—
Product1-(2,4,6-Trichlorophenyl)-2-acetyl-3-(2-chloro-5-myristoylaminoanilino)-3-pyrazolin-5-oneHCID 21394050—

Reaction Conditions

Temperature10 °C

Reaction Steps

1.07 g (0.01 mole) of lutidine is added to a solution of 30.7 g (0.05 mole) of 1-(2,4,6-trichlorophenyl)-3-(2-chloro-5-myristoylaminoanilino)-2-pyrazolin-5-one and 8 g (0.06 mole) of anhydrous aluminium chloride in 100 ml of dichloromethane. The solution is cooled to 10° C and 5.90 g (0.075 mole) of acetylchloride are added. 8 g (0.075 mole) of lutidine divided into 4 portions of 2 g each (one portion every 15 min) are added in a total period of time of 1 h, the temperature being kept below 10° C. The reaction mixture is stirred for 2 h more and then poured out into 1 l of 1N aqueous hydrochloric acid. The dichloromethane layer is washed until free from acid, dried, and concentrated by evaporation. The product is agitated with methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04061498
Source datasetuspto-grants-1977_12
ORD IDord-1e047ed0942046248435f195249898c6
Source noteuspto-grants-1977_12