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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 455406Generated: October 30, 2026

Triethylamine → HCID 178509447, compound

https://huagongshe.com/reaction/455406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantHCID 178513515HCID 178513515—
SolventDichloromethaneHCID 6344—
ProductHCID 178509447HCID 178509447—

Reaction Steps

Trifluoroacetic anhydride (0.4 mL) is added to a solution of cis-4-(1H-benzoimidazole-5-carbonyl)-1,2,3,4,4a,5,6,10b-octahydro-benzo[f]quinoline-8-carboxylic acid amide (140 mg) and triethylamine (0.6 mL) in dichloromethane (4 mL) chilled in an ice bath. The cooling bath is removed and the solution is stirred at room temperature for 3 h. Another portion of trifluoroacetic anhydride (0.4 mL) and triethylamine (0.6 mL) are then added and stirring is continued at 35° C. overnight. The solution is diluted with dichloromethane and washed with water and brine. After drying (MgSO4), the solvent is evaporated and the residue is chromatographed on silica gel (dichloromethane/methanol 20:1→1:1) to furnish the title compound as a yellowish solid. Yield: 50 mg (38% of theory); Mass spectrum (ESI+): m/z=357 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08497281B2
Source datasetuspto-grants-2013_07
ORD IDord-ca5662e9195248708ff4202e8cd7284b
Source noteuspto-grants-2013_07