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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353882Generated: October 30, 2026

1-Hydroxybenzotriazole → HCID 23512726, compound

https://huagongshe.com/reaction/353882

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantIsoquinoline-3-carboxylic acidHCID 124656—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-(4-aminobutyl)-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-4-amineHCID 22180872—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 23512726HCID 2351272629.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

Under a nitrogen atmosphere isoquinoline-3-carboxylic acid (1.32 g, 7.63 mmol), 1-hydroxybenzotriazole (1.12 g, 8.27 mmol), and dichloromethane (60 mL) were combined, allowed to stir for several minutes and then cooled to 0° C. 1-[3-(Dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride was added. Pyridine (1.8 mL) was added and the resulting mixture was allowed to stir for at least 60 minutes. A solution of 1-(4-aminobutyl)-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-4-amine (2.0 g, 6.37 mmol) in dichloromethane (250 mL) was added dropwise. The reaction mixture was allowed to stir at ambient temperature overnight. The reaction mixture was washed with sodium bicarbonate, dried over magnesium sulfate, filtered and then concentrated under reduced pressure. The crude material was purified by column chromatography (40 g silica gel eluting with dichloromethane/methanol 9/1) followed by recrystallization from methanol to provide 882 mg of N-{4-[4-amino-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-1-yl]butyl}isoquinoline-3-carboxamide as a yellow crystalline solid, m.p. 199-200° C. Analysis: Calculated for C27H28N6O2: % C, 69.21; % H, 6.02; % N, 17.94. Found: % C, 69.03; % H, 5.99; % N, 18.11.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06756382B2
Source datasetuspto-grants-2004_06
ORD IDord-856d15b83b474fbb81d4685a69526d06
Source noteuspto-grants-2004_06