HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851298Generated: October 31, 2026
Sodium Bicarbonate → 5-(4-{4-[5-(4-chloropyridine-2-yl)-1H-[1,2,4]triazole-3-yl]-piperidine-1-ylmethyl}-phenyl)-2-cyclopropyl-6-(4-fluorophenyl)-[1,2,4]triazolo[1,5-a]pyrimidine
https://huagongshe.com/reaction/1851298
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 2-Cyclopropyl-4-[6-(4-fluorophenyl)-[1,2,4]triazolo[1,5-a]pyrimidin-5-yl]-benzaldehyde | HCID 86703052 | — |
| Reactant | HCID 178478250 | HCID 178478250 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 5-(4-{4-[5-(4-chloropyridine-2-yl)-1H-[1,2,4]triazole-3-yl]-piperidine-1-ylmethyl}-phenyl)-2-cyclopropyl-6-(4-fluorophenyl)-[1,2,4]triazolo[1,5-a]pyrimidine | HCID 178505524 | 25.1% |
Reaction Steps
412 mg 4-Chloro-2-(5-piperidine-4-yl-2H-[1,2,4]triazole-3-yl)-pyridine×2HCl are dissolved in 7.2 mL NMP. After addition of 0.28 mL triethylamine the reaction mixture is stirred for one hour. 600 mg 2-Cyclopropyl-4-[6-(4-fluorophenyl)-[1,2,4]triazolo[1,5-a]pyrimidin-5-yl]-benzaldehyde (50% pure) and 0.09 mL acetic acid are added. The reaction mixture is stirred over night at room temperature. 191 mg (0.92 mmol) NaBH(OAc)3, are added in portions and the reaction mixture is stirred at room temperature for three days. After treatment of the reaction mixture with saturated NaHCO3 and stirring for one hour no solid precipitates. 200 mL tert.butyl-methylether are added and the mixture is stirred for one hour. After separation the organic phase is washed twice with water, dried and the solvent evaporated. Due to some remaining product in the aqueous phase this phase is extracted twice with tert.butyl-methylether (200 mL each). The combined organic phases are washed and dried. After removal of the solvent the residue is purified by chromatography on silica gel (dichloromethane/methanol). 134 mg (25.1%) of the pure product and additional 92.5 mg (18.2%) of the slightly contaminated product are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08957064B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-3a9dddeeee374b4ca7f2a1c32398db08 |
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| Source note | uspto-grants-2015_02 |
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