HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291077Generated: October 30, 2026
Trifluoroacetic acid → HCID 18919889, compound
https://huagongshe.com/reaction/1291077
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 2-Aminonicotinic acid | HCID 72930 | — |
| Reactant | 1-Benzylpiperidin-4-ol | HCID 78461 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18919889 | HCID 18919889 | 33.4% |
Reaction Steps
0.14 g (0.00101 mol) of 2-amino-nicotinic acid was suspended in 50 ml of THF and treated with 0.077 ml (0.00101 mol) of trifluoroacetic acid. The mixture was stirred at room temperature for 1 hr., whereby a solution resulted. To this was added 0.25 g (0.0015 mol) of carbonyidiimidazole and the mixture was stirred at room temperature for 2 hrs. Subsequently, 0.34 g (0.00178 mol) of 1-benyl-4-hydroxy-piperidine was added and the mixture was stirred at 60° for 72 hrs. After removing the solvent the residue was chromato-graphed over silica gel with ethyl acetate/hexane (1:1) as the eluent. 0.105 g (31%) of 1-benzyl-piperidin-4-yl 2-amino-nicotinate was obtained as white crystals. MS: me/e (% basic peak)=311 (C18H21N3O2+, 7.5), 173 (42), 91 (100), 82 (86).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05753679 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-33578e63dc914d1ca2d709c8ab08f154 |
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| Source note | uspto-grants-1998_05 |
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