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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856335Generated: October 29, 2026

2-Chloro-1-(2-methyloxiran-2-ylmethyl)-4-nitroimidazole → Tert-butyl{4-[3-(2-chloro-4-nitroimidazol-1-yl)-2-hydroxy-2-methylpropyl]piperazin-1-yl}carbamate

https://huagongshe.com/reaction/856335

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-1-(2-methyloxiran-2-ylmethyl)-4-nitroimidazoleHCID 15965523—
Reactanttert-Butyl piperazin-1-ylcarbamateHCID 21701658—
ProductTert-butyl{4-[3-(2-chloro-4-nitroimidazol-1-yl)-2-hydroxy-2-methylpropyl]piperazin-1-yl}carbamateHCID 9156068572.6%

Reaction Steps

Using 2-chloro-1-(2-methyloxiran-2-ylmethyl)-4-nitroimidazole prepared in Example 6 (4.36 g, 20.0 mmol) and tert-butyl piperazin-1-ylcarbamate (4.44 g, 22.0 mmol) gave tert-butyl{4-[3-(2-chloro-4-nitroimidazol-1-yl)-2-hydroxy-2-methylpropyl]piperazin-1-yl}carbamate (6.08 g, yield 72%) as a white powder in the same manner as in Example 365.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262212B2
Source datasetuspto-grants-2007_08
ORD IDord-9dafe8f904d74c33a196de3c4eeff170
Source noteuspto-grants-2007_08