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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368520Generated: October 31, 2026

Trifluoroacetic acid → HCID 71117564, compound

https://huagongshe.com/reaction/2368520

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 71117398HCID 71117398—
SolventDichloromethaneHCID 6344—
ProductHCID 71117564HCID 71117564—

Reaction Steps

To a solution of methyl 1-(4-fluorophenyl)-2-(tritylamino)-1H-imidazole-5-carboxylate (66) (200 mg, 0.419 mmol) in dichloromethane (10 mL) was added trifluoroacetic acid (5 mL). The reaction was stirred at room temperature overnight, concentrated and the residue was dissolved in ethyl acetate. The organic layer was washed with saturated sodium bicarbonate, brine, dried over sodium sulfate, filtered, and concentrated and in vacuo to afford methyl 2-amino-1-(4-fluorophenyl)-1H-imidazole-5-carboxylate (67) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703776B2
Source datasetuspto-grants-2014_04
ORD IDord-41f2cb3624f648018d91c8f7096e4104
Source noteuspto-grants-2014_04