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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534744Generated: October 27, 2026

Diisopropylethylamine → HCID 59262185, compound

https://huagongshe.com/reaction/534744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Fluoro-4-nitrobenzyl bromideHCID 2774661—
Reactanttert-Butyl (2S)-2-methylpiperazine-1-carboxylateHCID 10081508—
SolventDimethylformamideHCID 6228—
ProductHCID 59262185HCID 5926218592.5%

Reaction Steps

A solution of 4-(bromomethyl)-2-fluoro-1-nitrobenzene (232 mg, 1 mmol) and Hunig's base (0.192 mL, 1.1 mmol) in DMF (3 mL) was treated with 1,1-dimethylethyl (2S)-2-methyl-1-piperazinecarboxylate (200 mg, 1 mmol) in DMF (3 mL) and stirred at room temperature for 20 minutes. The reaction mixture was concentrated, re-dissolved in DCM and washed with water and brine, then dried and concentrated. The crude product was purified by column chromatography. Elution with EtOAc/pentane yielded the title compound as a colourless gum (327 mg). δH (CDCl3, 400 MHz) 8.03 (1H, m), 7.34 (1H, dd), 7.27 (1H, m), 4.22 (1H, br.s), 3.84 (1H, d), 3.58 (1H, d), 3.47 (1H, d), 3.13 (1H, td), 2.72 (1H, m), 2.54 (1H, m), 2.22 (1H, dd), 2.09 (1H, m), 1.46 (9H, s), 1.26 (3H, d) [values corrected for incorrectly referenced TMS at 0.62 ppm on spectrum].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853218B2
Source datasetuspto-grants-2014_10
ORD IDord-48993971b13a48aaa2c00c8ec0d8aa37
Source noteuspto-grants-2014_10