HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64485Generated: October 27, 2026
Potassium Carbonate → 1-{4-[({[8-(Cyclohexylmethoxy)-2-methylimidazo[1,2-a]pyridin-3-yl]carbonyl}amino)methyl]pyridin-2-yl}piperidine-4-carboxylic acid
https://huagongshe.com/reaction/64485
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Ethyl 4-piperidinecarboxylate | HCID 70770 | — |
| Reactant | N-[(6-chloropyridin-3-yl)methyl]-8-(cyclohexylmethoxy)-2-methylimidazo[1,2-a]pyridine-3-carboxamide | HCID 86713518 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-{4-[({[8-(Cyclohexylmethoxy)-2-methylimidazo[1,2-a]pyridin-3-yl]carbonyl}amino)methyl]pyridin-2-yl}piperidine-4-carboxylic acid | HCID 86713517 | — |
Reaction Steps
To a solution of 32 mg of N-[(6-chloropyridin-3-yl)methyl]-8-(cyclohexylmethoxy)-2-methylimidazo[1,2-a]pyridine-3-carboxamide in 0.6 ml of N-methyl-2-pyrrolidone was added 0.05 ml of ethyl piperidine-4-carboxylate to carry out a reaction at 150° C. for 30 minutes and further at 200° C. for 30 minutes under microwave irradiation. 24 mg of potassium carbonate was added thereto to carry out a reaction at 240° C. for 2 hours under microwave irradiation. To the reaction mixture were added a saturated aqueous ammonium chloride solution and ethyl acetate to carry out a layer separation operation. The organic layer was washed with water and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the obtained residue was purified by silica gel column chromatography. To the obtained purified product were added hexane and isopropyl ether, and the resulting solid was collected by filtration and dried to obtain 14 mg of 1-{4-[({[8-(cyclohexylmethoxy)-2-methylimidazo[1,2-a]pyridin-3-yl]carbonyl}amino)methyl]pyridin-2-yl}piperidine-4-carboxylic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09447090B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-72d58598dcac4f78ac5fa6e061a0dfdf |
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| Source note | uspto-grants-2016_09 |
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