HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 79366Generated: October 23, 2026
Imidazo(1,2-a)pyridine-3-carboxylic acid → N-(3-ethyl-1-((2-methoxy-6-methylpyridin-3-yl)methyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridine-3-carboxamide
https://huagongshe.com/en/reaction/79366
Participants
| Role | Name | HCID | Charge |
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| Reactant | Imidazo(1,2-a)pyridine-3-carboxylic acid | HCID 73142 | — |
| Reactant | DCM thionyl chloride | HCID 21879677 | — |
| Reactant | 3-ethyl-1-((2-methoxy-6-methylpyridin-3-yl)methyl)-1H-indazol-4-amine | HCID 67259597 | — |
| Solvent | Dce thf | HCID 21493386 | — |
| Product | N-(3-ethyl-1-((2-methoxy-6-methylpyridin-3-yl)methyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridine-3-carboxamide | HCID 67259571 | 35.9% |
Reaction Steps
To imidazo[1,2-a]pyridine-3-carboxylic acid (118 mg, 0.729 mmol) was added a mixture of 3:1 DCM/thionyl chloride (4 mL). The mixture was stirred at ambient temperature for 3 hours and then concentrated to a residue under N2 stream. The residue was dried under high vacuum for 30 minutes. 3-Ethyl-1-((2-methoxy-6-methylpyridin-3-yl)methyl)-1H-indazol-4-amine (108 mg, 0.364 mmol) in THF/DCE (1:1; 8 mL) was added to the dry acid-chloride residue. The reaction mixture was heated at 75° C. for 30 minutes. The mixture was concentrated under reduced pressure and diluted with DCM. The solution was washed with saturated NaHCO3 aqueous solution, dried (Na2SO4) and concentrated under reduced pressure. The residue was purified by silica gel chromatography eluting with 5% MeOH 0.5% NH4OH in DCM to give the product (57.6 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08841455B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-883da2428cfc48a3ba661eab93affe6c |
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| Source note | uspto-grants-2014_09 |
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