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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916827Generated: November 2, 2026

Toluene → 2-Amino-4-(3-carboxy-propyl)-imidazole-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1916827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantTrimethylaluminumHCID 16682925—
Reactant2-Amino-4-(3-methoxycarbonyl-propyl)-imidazole-1-carboxylic acid tert-butyl esterHCID 59766082—
Solvent1,2-DichloroethaneHCID 11—
SolventDichloromethaneHCID 6344—
Product2-Amino-4-(3-carboxy-propyl)-imidazole-1-carboxylic acid tert-butyl esterHCID 67061948—

Reaction Conditions

Temperature60 °C

Reaction Steps

General Aminolysis Procedure: To a stirring 0° C. solution of amine (0.704 mmol) in anhydrous 1,2-dichloroethane (1 mL) was added drop-wise a 2M solution of AlMe3 in PhCH3 (0.351 mL, 0.704 mmol). The solution was stirred for 10 min before the addition of 2-amino-4-(3-methoxycarbonyl-propyl)-imidazole-1-carboxylic acid tert-butyl ester 18 (100 mg, 0.352 mmol) in several portions. Once dissolution was complete, the reaction was warmed to 60° C. and stirred until completion as evident by TLC analysis. The reaction was then cooled back down to 0° C. before being diluted with dichloromethane (5 mL) and quenched with water (1 mL). The resulting viscous solution was warmed to ambient temperature and Celite® diatomite was added. After stirring for 5 min, the mixture was filtered and the filtrate washed with brine (2×3 mL), dried (Na2SO4), and evaporated to dryness. The crude product was purified via flash column chromatography (2-10% MeOH/CH2Cl2) to afford pure product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618149B2
Source datasetuspto-grants-2013_12
ORD IDord-88920c0de54d42aabb1b545ef6f02d54
Source noteuspto-grants-2013_12