HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266834Generated: October 25, 2026
3,4-Diaminopyridine → HCID 178525444, compound
https://huagongshe.com/reaction/266834
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3,4-Diaminopyridine | HCID 5918 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus oxide (P4O10) | HCID 14812 | — |
| Reactant | 1-{1-[4-(5-Carboxypentyloxy)benzoyl]-4-piperidinyl}-3,4-dihydrocarbostyril | HCID 19031046 | — |
| Product | HCID 178525444 | HCID 178525444 | — |
Reaction Steps
To 1-{1-[4-(5-carboxypentyloxy)benzoyl]-4-piperidinyl}-3,4-dihydrocarbostyril (2.00 g) are added 3,4-diaminopyridine (0.47 g), phosphorus pentoxide (1.00 g) and methanesulfonic acid (7.0 ml) and the mixture is stirred with heating at 100°-120° C. for 3 hours. After cooling, the reaction solution is poured into ice-water (30 ml) and the mixture is adjusted to around pH 11 with aqueous sodium hydroxide solution and extracted with dichloromethane. The extract is dried with magnesium sulfate and the solvent is distilled off. The resulting residue is purified by silica gel column chromatography (solvent: dichloromethane:methanol=20:1→9:1) to give 1-{1-[4-(5-(imidazo[4,5-c]pyridine-2-yl)carboxypentyloxy)benzoyl]-4-piperidinyl]-3,4-dihydrocarbostyril (1.32 g) as white amorphous form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05652247 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-435a73bbf412487a9679ff0200a53872 |
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| Source note | uspto-grants-1997_07 |
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