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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497928Generated: October 26, 2026

Trifluoroacetic acid → HCID 178509455, compound

https://huagongshe.com/reaction/497928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantTriethylsilaneHCID 12052—
Reactant1H-Imidazole-4-carbaldehydeHCID 76428—
Reactant(R)-2,3,4,5-tetrahydro-3-(phenylmethyl)-4-(2-thienylsulfonyl)-1H-1,4-benzodiazepine-7-carbonitrileHCID 10740273—
SolventTolueneHCID 1140—
ProductHCID 178509455HCID 178509455100%

Reaction Conditions

Temperature22.5 °C

Reaction Steps

(R)-2,3,4,5-tetrahydro-3-(phenylmethyl)-4-(2-thienylsulfonyl)-1H- 1,4-benzodiazepine-7-carbonitrile (10 g) and imidazole-4-carboxaldehyde (2.6 g) were mixed in toluene (20 mL) at 20 to 25° C. To this stirred slurry, first trifluoroacetic acid (9.4 mL) and then trifluoroacetic acid anhydride (5.2 mL) were added sequentially while maintaining the temperature below 30° C. The biphasic mixture was vigorously stirred at 20 to 25° C. for 2 hours. Triethylsilane was then added and the reaction mixture was stirred at 20 to 25° C. until the reaction was determined to be complete according to HPLC assay. The reaction mixture was polish-filtered, e.g., through filter paper or a celite bed. The solvent was removed by evaporation, and a viscous yellow oil containing approximately 100% yield of the crude title product was collected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06949642B2
Source datasetuspto-grants-2005_09
ORD IDord-30a5194cb46d441dad499f0601af3734
Source noteuspto-grants-2005_09