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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6914Generated: October 29, 2026

Benzylamine → 4-(4-Benzyl-5-methyl-4H-[1,2,4]triazol-3-yl)-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/6914

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
Reactant1-Boc-4-(5-methyl-1,3,4-oxadiazol-2-yl)piperidineHCID 21098364—
CatalystMagnesium ChlorideHCID 5360315—
Product4-(4-Benzyl-5-methyl-4H-[1,2,4]triazol-3-yl)-piperidine-1-carboxylic acid tert-butyl esterHCID 2354407170.4%

Reaction Conditions

Temperature150 °C

Reaction Steps

4-(5-Methyl-[1,3,4]oxadiazol-2-yl)-piperidine-1-carboxylic acid tert-butyl ester (5 g, 18.7 mmol) (see reference WO 0039125), benzylamine (2.5 ml, 22 mmol) and magnesium chloride (100 mg) were heated at 150° C. for 1 hour, a further quantity of benzylamine (2.5 ml, 22 mmol) was added and the mixture was heated at 150° C. for 4 hours. The reaction mixture was cooled to room temperature and the reaction mixture was purified by chromatography on silica gel using methanol in dichloromethane as eluant (3:97). The material isolated was triturated with diethyl ether to give the title compound as a white solid (4.69 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07084145B2
Source datasetuspto-grants-2006_08
ORD IDord-f6db3128a3104baab6ac26020f6aaa80
Source noteuspto-grants-2006_08