HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1915580Generated: October 30, 2026
Pyridine-2-carbonitrile → HCID 178432371, compound
https://huagongshe.com/reaction/1915580
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine-2-carbonitrile | HCID 7522 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | tert-Butyl 4-(hydrazinecarbonyl)piperidine-1-carboxylate | HCID 22713165 | — |
| Reactant | HCID 86630684 | HCID 86630684 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 178432371 | HCID 178432371 | — |
Reaction Steps
0.49 ml triethylamine is added to a solution of 0.55 g 2-(5-piperidin-4H[1,2,4]triazol-3-yl)-pyridine*2HCl (prepared from tert-butyl 4-(hydrazinocarbonyl)piperidine-1-carboxylate and pyridine-2-carbonitrile according to a procedure described in U.S. Pat. No. 4,011,218 or WO2005100344) in 15 ml methanol. To this solution a solution of 0.50 g 4-(2,7-dimethyl-6-phenyl[1,2,4]triazolo[1,5-a]pyrimidin-5-yl)benzaldehyde in 15 ml DMF is added, followed by 0.23 ml glacial acetic acid and 0.64 g NaBH(OAc)3. The resulting mixture is stirred at room temperature. Additional portions of 2 equivalents NaBH(OAc)3 are added after 1, 2, 3, 5 and 7 h. The solvent is removed by evaporation after 20 h and the residue is purified by chromatography on silica gel (dichloromethane/[dichloromethane+7M NH3 in methanol]) to yield the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08614218B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-0bdc57ef5cd7439f88475f00cdfc4ef7 |
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| Source note | uspto-grants-2013_12 |
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