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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856297Generated: October 30, 2026

Dimethylformamide → HCID 69635160, compound

https://huagongshe.com/reaction/856297

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantHCID 10104781HCID 10104781—
SolventWaterHCID 962—
ProductHCID 69635160HCID 6963516081.1%

Reaction Conditions

Temperature57.5 °C

Reaction Steps

A mixture of (S)-2-chloro-1-(2-methyloxiran-2-ylmethyl)-4-nitroimidazole prepared in Example 18 (440 mg, 2.02 mmol), tert-butyl piperazine-1-carboxylate (414 mg, 2.22 mmol) and DMF (4 ml) was stirred at 55-60° C. for 9 hours. The reaction mixture was allowed to return to room temperature, then diluted with water (24 ml), and the solution was extracted with ethyl acetate (10 ml) twice. The organic phases were combined, washed with water (20 ml) three times and a saturated saline solution (10 ml), dried over sodium sulfate and then filtered. The filtrate was concentrated under reduced pressure, and the residue treated with diethyl ether to afford tert-butyl (R)-4-[3-(2-chloro-4-nitroimidazol-1-yl)-2-hydroxy-2-methylpropyl]piperazine-1-carboxylate (662 mg, yield 81%) as a light yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262212B2
Source datasetuspto-grants-2007_08
ORD IDord-e030abad630347468b93ef58ff355e25
Source noteuspto-grants-2007_08