HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487970Generated: October 31, 2026
Ethanol → Methyl 4-cyclopropyl-5-(3H-imidazo[4,5-c]pyridin-2-yl)-2-methylbenzoate
https://huagongshe.com/reaction/1487970
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | 3,4-Diaminopyridine | HCID 5918 | — |
| Reactant | Methyl 4-cyclopropyl-5-formyl-2-methylbenzoate | HCID 90021238 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | Methyl 4-cyclopropyl-5-(3H-imidazo[4,5-c]pyridin-2-yl)-2-methylbenzoate | HCID 90021751 | 38.1% |
Reaction Steps
Into a 100-mL round-bottom flask was placed a mixture of methyl 4-cyclopropyl-5-formyl-2-methylbenzoate (compound 87.1, 500 mg, 2.29 mmol), pyridine-3,4-diamine (500 mg, 4.58 mmol), NH4OAc (1.42 g, 18.4 mmol) and ethanol (50 mL). The resulting mixture was stirred open to the air for 3 days at 70° C., then cooled to room temperature and diluted with aqueous sodium bicarbonate (sat., 50 mL). The aqueous phase was extracted with ethyl acetate (2×50 mL) and the combined organic layers were dried (Na2SO4), filtered, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography with ethyl acetate as the eluent to yield 268 mg (38%) of the title compound as a yellow semi-solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09428502B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-0f440eda1935477abfbf00d5a05b26d0 |
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| Source note | uspto-grants-2016_08 |
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