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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245493Generated: November 1, 2026

Triethylamine → 2-[3,5-Bis(trifluoromethyl)phenyl]-n{4-(4-fluoro-2-methylphenyl)-6-[(7as)-3-oxotetrahydro-1h-pyrrolo[1,2-c]imidazol-2(3h)-yl]-3-pyridinyl}-n,2-dimethylpropanamide

https://huagongshe.com/reaction/2245493

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTriphosgeneHCID 94429—
Reactant2-[3,5-bis(trifluoromethyl)phenyl]-N-(4-(4-fluoro-2-methylphenyl)-6-{[(2S)-2-pyrrolidinylmethyl]amino}-3-pyridinyl)-N,2-dimethylpropanamideHCID 59215770—
SolventDichloromethaneHCID 6344—
Product2-[3,5-Bis(trifluoromethyl)phenyl]-n{4-(4-fluoro-2-methylphenyl)-6-[(7as)-3-oxotetrahydro-1h-pyrrolo[1,2-c]imidazol-2(3h)-yl]-3-pyridinyl}-n,2-dimethylpropanamideHCID 1606399937.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

The starting 2-[3,5-bis(trifluoromethyl)phenyl]-N-(4-(4-fluoro-2-methylphenyl)-6-{[(2S)-2-pyrrolidinylmethyl]amino}-3-pyridinyl)-N,2-dimethylpropanamide (D62, 38 mg, 0.064 mmol) was dissolved in 1 mL of anhydrous dichloromethane and treated with triethylamine (20 μL, 0.143 mmol). The solution was brought to 0° C. and triphosgene (10 mg, 0.034 mmol) was added. The reaction was stirred at 0° C. for 15 min, then brought to room temperature. After 24 h, the reaction was diluted with dichloromethane (10 mL) and extracted with brine. The organics were collected and the solvent removed. The product was isolated by flash chromatography (silica, cyclohexane: EtOAc 80:20 to EtOAc). Thus were obtained 8 mg of the target compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07683056B2
Source datasetuspto-grants-2010_03
ORD IDord-71a0aa2ad34f46f2acf1df488f2cadf0
Source noteuspto-grants-2010_03