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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274012Generated: October 30, 2026

Methyl 5-Amino-2-chlorobenzoate → methyl 2-chloro-5-({[1-methyl-3-(pentafluoroethyl)-4-(trifluoromethyl)-1H-pyrazol-5-yl]carbonyl}amino)benzoate

https://huagongshe.com/reaction/2274012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 5-Amino-2-chlorobenzoateHCID 5200412—
Reactant1-methyl-3-(pentafluoroethyl)-4-(trifluoromethyl)-1H-pyrazole-5-carbonyl chlorideHCID 86660074—
CatalystCID 101611454HCID 178509332—
SolventDichloromethaneHCID 6344—
Productmethyl 2-chloro-5-({[1-methyl-3-(pentafluoroethyl)-4-(trifluoromethyl)-1H-pyrazol-5-yl]carbonyl}amino)benzoateHCID 86660079—

Reaction Steps

A solution of 4.24 g (12.8 mmol) of 1-methyl-3-(pentafluoroethyl)-4-(trifluoromethyl)-1H-pyrazole-5-carbonyl chloride in 25 ml of dichloromethane p.a. is added to a suspension of 2.38 g (12.8 mmol) of methyl 5-amino-2-chlorobenzoate and 2.57 g (19.2 mmol) of silver(I) cyanide in 50 ml of dichlormethane p.a., and the mixture is stirred at room temperature for 16 h. The suspension is then filtered through silica gel and the product is eluted using a mixture of cyclohexane and ethyl acetate (1:1). The organic phase is washed successively three times with 6N hydrochloric acid and twice with saturated sodium chloride solution. The organic phase is then dried over sodium sulphate, filtered and concentrated on a rotary evaporator under reduced pressure. This gives 5.75 g (93%) of methyl 2-chloro-5-({[1-methyl-3-(pentafluoroethyl)-4-(trifluoromethyl)-1H-pyrazol-5-yl]carbonyl}amino)benzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126945B2
Source datasetuspto-grants-2015_09
ORD IDord-946cc60b37e244af9d34224f11fde5de
Source noteuspto-grants-2015_09