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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266834Generated: October 25, 2026

3,4-Diaminopyridine → HCID 178525444, compound

https://huagongshe.com/reaction/266834

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-DiaminopyridineHCID 5918—
ReactantMethanesulfonic AcidHCID 6395—
ReactantSodium HydroxideHCID 14798—
ReactantPhosphorus oxide (P4O10)HCID 14812—
Reactant1-{1-[4-(5-Carboxypentyloxy)benzoyl]-4-piperidinyl}-3,4-dihydrocarbostyrilHCID 19031046—
ProductHCID 178525444HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05652247
Source datasetuspto-grants-1997_07
ORD IDord-435a73bbf412487a9679ff0200a53872
Source noteuspto-grants-1997_07