HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 986663Generated: October 30, 2026
4-Aminopyridine → HCID 70381943, compound
https://huagongshe.com/reaction/986663
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Aminopyridine | HCID 1727 | — |
| Reactant | 2-Chloromethylbenzimidazole | HCID 78571 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 70381943 | HCID 70381943 | 113.1% |
Reaction Steps
A solution of 1.665 g (10 m mol) of 2- chloromethybenzimidazole and 1.88 g (20 m mol) of 4- aminopyridine in 20 ml of ethanol was refluxed under heating for three hours. The solution was evaporated in vacuo to a dark oil, dissolved in 20 ml of water and washed twice with 20 ml of ethylacetate The aqueous phase was evaporated in vacuo. The residual oil was dissolved in 3 ml of concentrated hydrochloric acid and chilled (0° C.) causing a crystalline precipitate to form. The crystals were filtered with the aid of ethanol. Recrystallization from methanol gave 1.68 g (53.3%) of the title compound (I).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04714764 |
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| Source dataset | uspto-grants-1987_12 |
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| ORD ID | ord-07c970f2191141729624b113c9814452 |
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| Source note | uspto-grants-1987_12 |
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