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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2063462Generated: November 2, 2026

Diisopropylethylamine → (R)-2-(4-(4-chlorobenzyl)-5-ethyl-4H-1,2,4-triazol-3-yl)-N-((S)-7-(trifluoromethyl)chroman-4-yl)pyrrolidine-1-carboxamide

https://huagongshe.com/reaction/2063462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantTriphosgeneHCID 94429—
ReactantSodium BicarbonateHCID 516892—
Reactant(S)-7-(trifluoromethyl)chroman-4-amineHCID 46911908—
Reactant(R)-4-(4-chlorobenzyl)-3-ethyl-5-(pyrrolidin-2-yl)-4H-1,2,4-triazole HCl saltHCID 68811647—
SolventDichloromethaneHCID 6344—
SolventSodium chloride; waterHCID 57417360—
Product(R)-2-(4-(4-chlorobenzyl)-5-ethyl-4H-1,2,4-triazol-3-yl)-N-((S)-7-(trifluoromethyl)chroman-4-yl)pyrrolidine-1-carboxamideHCID 57650136276%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirring solution of triphosgene (14.87 mg, 0.05 mmol) in 8 mL of CH2Cl2 at 0° C. was added dropwise a mixed solution of (S)-7-(trifluoromethyl)chroman-4-amine (32.58 mg, 0.15 mmol) and N,N-diisopropylethylamine (0.07841 mL, 0.45 mmol) in dichloromethane (2 mL). The reaction mixture was stirred at 0° C. for 30 minutes. Then to the mixture at 0° C. was added a solution of the (R)-4-(4-chlorobenzyl)-3-ethyl-5-(pyrrolidin-2-yl)-4H-1,2,4-triazole HCl salt (54.57 mg, 0.15 mmol) and N,N-diisopropylethylamine (0.07841 mL, 0.45 mmol) in dichloromethane (2 mL) slowly. The resulting mixture was stirred 0° C. for 30 minutes, then at room temperature overnight. The reaction mixture was treated with sat. aqueous NaHCO3 (10 mL) and brine, dried over Na2SO4, and concentrated in vacuo. Flash chromatography purification (Hex/EtOAc gradient, 10-100% EtOAc with 10% MeOH) afforded the desired product as a white solid (73.7 mg, 92.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288371B2
Source datasetuspto-grants-2012_10
ORD IDord-654726d74cfa4caaa9ec970169430061
Source noteuspto-grants-2012_10