HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 3-(Cyclopropylmethyl)-7-(4-phenyl-1-piperidinyl)-1,2,4-triazolo[4,3-a]pyridine-8-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Phenylpiperidine | HCID 69873 | — |
| Reactant | 7-Chloro-3-(cyclopropylmethyl)[1,2,4]triazolo[4,3-a]pyridine-8-carbonitrile | HCID 57459593 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-(Cyclopropylmethyl)-7-(4-phenyl-1-piperidinyl)-1,2,4-triazolo[4,3-a]pyridine-8-carbonitrile | HCID 57459636 | 49% |
Reaction Conditions
| Temperature | 150 °C |
|---|
Reaction Steps
A mixture of compound D5 (0.2 g, 0.86 mmol), 4-phenylpiperidine (0.166 g, 1.031 mmol), K2CO3 (0.148 g, 1.074 mmol) in CH3CN (5 ml) was heated in a sealed tube at 150° C. under microwave irradiation for 5 min. The mixture was then cooled to r.t. and the solvents evaporated in vacuo. The residue thus obtained was purified by column chromatography (silica gel; DCM/7M solution of NH3 in MeOH up to 3% as eluent). The desired fractions were collected and concentrated in vacuo to yield compound E13 as yellow solid (0.150 g, 49%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08937060B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-6d2c4b81a83542159374bad5c7e74e88 |
| Source note | uspto-grants-2015_01 |