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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241799Generated: October 27, 2026

Diisopropylethylamine → methyl 4-(4-nitro-2,3-dihydro-1H-inden-1-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/241799

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethyl piperazine-1-carboxylate hydrochlorideHCID 18399648—
Reactant1-chloro-4-nitro-2,3-dihydro-1H-indeneHCID 59302729—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Productmethyl 4-(4-nitro-2,3-dihydro-1H-inden-1-yl)piperazine-1-carboxylateHCID 5930272578%

Reaction Conditions

Temperature79 °C

Reaction Steps

To a room temperature solution of 1-Chloro-4-nitro-2,3-dihydro-1H-indene (221 mg, 1.12 mmol, 1.0 equiv) and DIPEA (430 μL, 2.46 mmol, 2.2 equiv) in dry acetonitrile (1.6 mL) was added methylpiperazine carboxylate hydrochloride salt (444 mg, 2.46 mmol, 2.2 equiv) as a solid in one portion. The resulting reaction mixture was heated to 79° C. overnight. The reaction mixture was allowed to cool to RT and diluted with EtOAc. The organic layer was extracted with 1 M HCl (3×20 mL), and the combined aqueous layers were treated with 3 N NaOH until the pH=10. The resulting solution was extracted three times with EtOAc, and the combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo to provide the title compound as a brown oil (239 mg, 78%). LCMS [M+H]+=306.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653081B2
Source datasetuspto-grants-2014_02
ORD IDord-f6111a8b74104884ac40d923feb071c7
Source noteuspto-grants-2014_02