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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466073Generated: November 3, 2026

Tetrahydrofuran → tert-Butyl 6-methoxy-2-methyl3-[{2-oxopiperazin-1-yl}acetyl]benzonitrile

https://huagongshe.com/reaction/1466073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantLithium diisopropylamideHCID 2724682—
ReactantTert-butyl 3-oxopiperazine-1-carboxylateHCID 3157178—
Reactant3-(Bromoacetyl)-6-methoxy-2-methylbenzonitrileHCID 89525026—
Producttert-Butyl 6-methoxy-2-methyl3-[{2-oxopiperazin-1-yl}acetyl]benzonitrileHCID 131732686—

Reaction Steps

To a THF solution of tert-butyl 3-oxopiperazine-1-carboxylate (0.082 g, 0.41 mmol) was added Lithium diisopropylamide (0.24 mL, 0.39 mmol) dropwise at −78° C. After stirring for 15 minutes, a THF solution of 3-(Bromoacetyl)-6-methoxy-2-methylbenzonitrile (0.10 g, 0.37 mmol) was added to the reaction mixture slowly. Analysis of the reaction mixture by LC indicated formation of the desired product. To the reaction mixture was added saturated NH4Cl, followed by extraction of the aqueous layer with EtOAc. The combined extracts were washed with brine, dried over Na2SO4, and concentrated under reduced pressure to provide a residue which was purified by silica gel column chromatography to provide the title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999990B2
Source datasetuspto-grants-2015_04
ORD IDord-9f56e075eedf42a4a1a1063280809d6a
Source noteuspto-grants-2015_04