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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl 5-Amino-2-chlorobenzoate | HCID 5200412 | — |
| Reactant | 1-methyl-3-(pentafluoroethyl)-4-(trifluoromethyl)-1H-pyrazole-5-carbonyl chloride | HCID 86660074 | — |
| Catalyst | CID 101611454 | HCID 178509332 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | methyl 2-chloro-5-({[1-methyl-3-(pentafluoroethyl)-4-(trifluoromethyl)-1H-pyrazol-5-yl]carbonyl}amino)benzoate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09126945B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-946cc60b37e244af9d34224f11fde5de |
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| Source note | uspto-grants-2015_09 |
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