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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280503Generated: October 31, 2026

Pyridine → HCID 178441564, compound

https://huagongshe.com/reaction/1280503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantHCID 22180889HCID 22180889—
ReactantHCID 131723488HCID 131723488—
ProductHCID 178441564HCID 178441564—

Reaction Steps

A solution of N-hydroxysuccinimidoiminobiotin (0.74 g, 1.76 mmol) in pyridine (10 mL) was slowly added to a solution of 1-(2-aminoethyl)-2-butyl-1H-imidazo[4,5-c]quinolin-4-amine (0.50 g, 1.76 mmol) in pyridine (30 mL). The reaction was maintained at ambient temperature overnight and then concentrated to dryness. The residue was partitioned between dichloromethane and aqueous saturated potassium carbonate. The organic layer was dried over magnesium sulfate and then concentrated to dryness. The residue was recrystallized from ethanol to provide 0.5 g of N1-[2-(4-amino-2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)ethyl]-5-(2-iminoperhydrothieno[3,4-d]imidazol-4-yl)pentanamide as a solid, m.p. 95-96° C. High resolution mass spec: Theoretical mass=508.2733, Measured mass=508.2723.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451810B1
Source datasetuspto-grants-2002_09
ORD IDord-8322a4f484b247f59478d8de745e6d76
Source noteuspto-grants-2002_09