HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615653Generated: November 1, 2026
Trifluoroacetic acid → HCID 178425982, compound
https://huagongshe.com/reaction/1615653
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 1,1-Dimethylethyl (((2,4,6-trimethylphenyl)sulphonyl)oxy)carbamate | HCID 359285 | — |
| Reactant | 1,6-Naphthyridin-5-amine | HCID 29249622 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178425982 | HCID 178425982 | — |
Reaction Steps
To trifluoroacetic acid (10 mL), stirred at 0° C., was added tert-butyl mesitylsulfonyloxycarbamate (6.50 g, 20.6 mmol), and the mixture was stirred at 0° C. for 30 min. The mixture was poured into ice-water (10 mL). A white precipitate was formed, which was filtered and collected. The white precipitate was dissolved in DCM (20 mL), and dried with Na2SO4. To the DCM solution was added 1,6-naphthyridin-5-amine (1.0 g, 6.88 mmol), and the mixture was stirred at room temperature for 4 h. The solvent was removed under reduced pressure and the residue was washed with Et2O (3×15 mL). The yellow solid obtained was used in the next step without further purification (3.30 g). ESI MS: m/z 161 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08765760B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-78d29409061b4259a66ee0da5ea22ebd |
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| Source note | uspto-grants-2014_07 |
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