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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701042Generated: October 30, 2026

Trifluoroacetic acid → HCID 53913605, compound

https://huagongshe.com/reaction/1701042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 53673637HCID 53673637—
SolventDichloromethaneHCID 6344—
ProductHCID 53913605HCID 5391360599.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

((1R)-1-(5-Carbamoyl-[1,3,4]oxadiazol-2-yl)-2-phenylethyl)methylcarbamic acid tert-butylester (350 mg, 1.01 mmol) was dissolved in dichloromethane (6 ml). The solution was cooled to 0° C. Trifluoroacetic acid (2 ml) was added dropwise. The solution was stirred for 30 min. The solvent was removed in vacuo. The residue was dissolved in dichloromethane (6 ml) and the solvent was removed in vacuo. The residue was again dissolved in dichloromethane (6 ml) and the solvent was removed in vacuo. The residue was dissolved in dichloromethane (10 ml). This phase was washed with water. The aqueous phase was lyophilized to give 247 mg of crude 5-((1R)-1-methylamino-2-phenylethyl)-[1,3,4]oxadiazole-2-carboxylic acid amide, which was used for the further synthesis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06350767B1
Source datasetuspto-grants-2002_02
ORD IDord-70bbf5a8a99e49d58f4dc94c1b9129b7
Source noteuspto-grants-2002_02