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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274004Generated: October 30, 2026

Diisopropylethylamine → HCID 88951200, compound

https://huagongshe.com/reaction/2274004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Amino-1-cyclopropanecarbonitrile hydrochlorideHCID 14586363—
ReactantHCID 86713745HCID 86713745—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 88951200HCID 88951200—

Reaction Steps

68.3 mg (0.58 mmol) of 1-aminocyclopropanecarbonitrile hydrochloride are initially charged in 5.0 ml of dichloromethane p.a., and 0.148 ml (0.86 mmol) of N-ethyldiisopropylamine and 156 mg of 2-chloro-5-(methyl{[1-methyl-3,4-bis(trifluoromethyl)-1H-pyrazol-5-yl]carbonyl}amino)benzoyl chloride (0.29 mmol) dissolved in 5.0 ml of dichloromethane p.a. are then added in succession. The reaction is stirred at room temperature for 16 hours. The reaction solution is diluted with 30 ml of ethyl acetate. The organic phase is washed twice with 1 N hydrochloric acid, once with 1 N aqueous sodium hydroxide solution and once with saturated sodium chloride solution. The organic phase is dried over magnesium sulphate and filtered and the solvent is removed on a rotary evaporator under reduced pressure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126945B2
Source datasetuspto-grants-2015_09
ORD IDord-5c18a57325b7441d943a7c66d21e268d
Source noteuspto-grants-2015_09