HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701042Generated: October 30, 2026
Trifluoroacetic acid → HCID 53913605, compound
https://huagongshe.com/reaction/1701042
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 53673637 | HCID 53673637 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 53913605 | HCID 53913605 | 99.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06350767B1 |
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| Source dataset | uspto-grants-2002_02 |
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| ORD ID | ord-70bbf5a8a99e49d58f4dc94c1b9129b7 |
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| Source note | uspto-grants-2002_02 |
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