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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 380396Generated: October 30, 2026

Diisopropylamine → HCID 178491390, compound

https://huagongshe.com/reaction/380396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
Reactant4-MethylpyridineHCID 7963—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178498256HCID 178498256—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178491390HCID 178491390—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of diisopropylamine (0.47 ml) in tetrahydrofuran (6 ml), cooled to −10° C., was treated dropwise, with a solution of butyl lithium in hexanes (1.2 ml, 2.5M). The resulting solution was stirred for 10 minutes, then cooled to −78° C. and then treated dropwise with a solution of 4-picoline (0.29 ml) in tetrahydrofuran (1 ml). This solution was stirred for 30 minutes then treated with a solution of methyl 2-cyclopentyl-7-methoxy-3H-benzimidazole-4-carboxylate [0.274 g, Reference Example 3(t)] in tetrahydrofuran (2 ml). The cold bath was removed and the reaction mixture stirred for 15 minutes at ambient temperature. The mixture was quenched with water, then diluted with ethyl acetate. The organic phase was separated then washed with brine, then dried over magnesium sulphate and then evaporated. The residue was subjected to flash chromatography on silica, eluting with a mixture of methanol and dichloromethane (8:92,v/v), to give the title compound (0.126 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06303600B1
Source datasetuspto-grants-2001_10
ORD IDord-71426e4081fa4593a4034b6c446e91df
Source noteuspto-grants-2001_10