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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2084918Generated: November 1, 2026

Trifluoroacetic acid → HCID 9798637, compound

https://huagongshe.com/reaction/2084918

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 9890137HCID 9890137—
SolventDichloromethaneHCID 6344—
ProductHCID 9798637HCID 9798637—

Reaction Steps

To a solution of 0.147 g (0.325 mmol) of the product of Example 58, 4-(4-but-2-ynyloxy-benzenesulfonyl)-3-hydroxycarbamoyl-piperazine-1-carboxylic acid tert-butyl ester, in 3.0 mL of dichloromethane was added 0.3 mL of trifluoroacetic acid and the reaction was stirred at room temperature for 1 h. The reaction was then concentrated in vacuo and the residue was diluted with dichloromethane. The organics were washed with saturated sodium bicarbonate solution, dried over sodium sulfate, filtered and concentrated in vacuo to provide 0.053 g of 1-(4-but-2-ynyloxy-benzenesulfonyl)-piperazine-2-carboxylic acid hydroxyamide as a tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06716833B2
Source datasetuspto-grants-2004_04
ORD IDord-cc9443af2ae84c64aa1a0387344ca889
Source noteuspto-grants-2004_04