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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729655Generated: October 29, 2026

Imidazole → HCID 66701989, compound

https://huagongshe.com/reaction/729655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant(R)-(-)-2-Amino-1-propanolHCID 80308—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 85927987HCID 85927987—
SolventTetrahydrofuranHCID 8028—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 66701989HCID 66701989—

Reaction Steps

N,N-Diisopropylethylamine (5.2 ml) was added to a solution of (R)-alaninol (2.56 ml) and the subtitle product of step ii) in NMP (35 ml) and stirred at 100° C. for 24 h and then 140° C. for 24 h. After cooling to ambient temperature imidazole (2.60 g) and a solution of tert-butyldimethylsilyl chloride (2.60 g) in THF (10 ml) were added and stirring maintained for 1 h. The volatiles were removed in vacuo and the residue was purified by column chromatography (1:1 Et2O/iso-hexane) to afford the subtitle compound as a yellow oil. Yield: 1.70 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582644B2
Source datasetuspto-grants-2009_09
ORD IDord-b6883046849f4547baa8100ea9c00517
Source noteuspto-grants-2009_09