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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892532Generated: November 1, 2026

Trifluoroacetic acid → HCID 86650038, compound

https://huagongshe.com/reaction/1892532

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 86762012HCID 86762012—
SolventDichloromethaneHCID 6344—
ProductHCID 86650038HCID 8665003882%

Reaction Steps

To a solution of tert-butyl 2-{[2-(4-{[2-(acetylamino)-1,3-thiazol-4-yl]methoxy}phenyl)ethyl]carbamoyl}hydrazinecarboxylate (305.0 mg, 0.667 mmol) in anhydrous dichloromethane (20 ml) was added trifluoroacetic acid (2.48 ml, 33.4 mmol) at 0° C. The reaction mixture was stirred at room temperature for 2 hr,and concentrated under reduced pressure. Dichloromethane (20 ml) was added to the residue and the mixture was concentrated again under reduced pressure. This operation was repeated 3 times to remove trifluoroacetic acid azeotropically. Ethyl acetate (30 ml) was added to the residue and the mixture was stirred. The precipitate was collected by filtration, washed 5 times with ethyl acetate and 5 times with diethyl ether, and dried under reduced pressure to give the title compound (253.4 mg, 0.547 mmol, yield 81.9%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507690B2
Source datasetuspto-grants-2013_08
ORD IDord-ef545ed165ee42a68deb2eaf3b464e01
Source noteuspto-grants-2013_08