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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856339Generated: October 29, 2026

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

https://huagongshe.com/reaction/856339

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-2-chloro-1-(2-methyloxiran-2-ylmethyl)-4-nitroimidazoleHCID 10443353—
Reactanttert-Butyl piperazin-1-ylcarbamateHCID 21701658—
Producttert-butyl (S)-{4-[3-(2-chloro-4-nitroimidazol-1-yl)-2-hydroxy-2-methylpropyl]piperazin-1-yl}carbamateHCID 8676053764%

Reaction Steps

Using (R)-2-chloro-1-(2-methyloxiran-2-ylmethyl)-4-nitroimidazole prepared in Example 12 (29.8 g, 137 mmol) and tert-butyl piperazin-1-ylcarbamate (28.9 g, 144 mmol) gave tert-butyl (S)-{4-[3-(2-chloro-4-nitroimidazol-1-yl)-2-hydroxy-2-methylpropyl]piperazin-1-yl}carbamate (36.68 g, yield 64%) as a white powder in the same manner as in Example 496.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262212B2
Source datasetuspto-grants-2007_08
ORD IDord-1c523f11395b4c99b62cc6f75a5cc47a
Source noteuspto-grants-2007_08