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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376050Generated: November 4, 2026

Trifluoroacetic acid → HCID 58786451, compound

https://huagongshe.com/reaction/1376050

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 58786450HCID 58786450—
SolventDichloromethaneHCID 6344—
ProductHCID 58786451HCID 5878645183%

Reaction Steps

To 4-[1-(2,4-Difluoro-phenyl)-2-methoxycarbonylamino-ethyl]-piperazine-1-carboxylic acid tert-butyl ester (420) (0.225 g, 0.564 mmol) in MeCl2 (2.0 mL) was added TFA (2.0 mL). The reaction was allowed to stir at room temperature for 1 h. The reaction mixture was concentrated to dryness. The resulting residue was taken up in 1N HCl (30 mL) and washed with EtOAc (30 mL). The aqueous layer was made alkaline with 5N NaOH (10 mL) and the desired product was extracted into EtOAc. The organic phase was concentrated to dryness yielding 0.14 g (83%) pure product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169777B2
Source datasetuspto-grants-2007_01
ORD IDord-b2e32432f0724d9bb222ecd830a8c153
Source noteuspto-grants-2007_01