HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201711Generated: October 29, 2026
Trifluoroacetic acid → HCID 86712538, compound
https://huagongshe.com/reaction/2201711
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 71007264 | HCID 71007264 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86712538 | HCID 86712538 | 55% |
Reaction Steps
To a solution of tert-butyl (2-(2-amino-2-oxoacetamido)-4-(thiophen-2-yl)phenyl)carbamate (0.1 g, 0.28 mmol) in DCM (3 mL) was added TFA (1 mL, 13 mmol) at 0° C. The reaction was warmed to room temperature and stirred for 2 h. The reaction was then concentrated under reduced pressure. The residue was basified with a saturated aqueous solution of Na2CO3. The obtained solid was filtered, washed with water and ether then dried to afford N1-(2-amino-5-(thiophen-2-yl)phenyl)oxalamide (40 mg, 55% yield). ESI+ MS: m/z 262 ([M+H]+), 1H NMR (500 MHz, d6-DMSO): δ 9.89 (s, 1H), 8.24 (s, 1H), 7.94 (s, 1H), 7.59 (d, J=2.0 Hz, 1H), 7.6 (d, J=5 Hz, 1H), 7.29-7.26 (m, 1H), 7.23 (d, J=4.0 Hz, 1H), 7.05 (t, J=4.0 Hz, 1H), 6.80 (d, J=9.0 Hz, 1H), 5.16 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09365498B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-daca6e0893da4485a16ed345314d846f |
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| Source note | uspto-grants-2016_06 |
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