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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993634Generated: October 30, 2026

Water → 1-Boc-4-(6-methyl-5-nitro-2-pyridinyl)-piperazine

https://huagongshe.com/reaction/1993634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant6-Chloro-2-methyl-3-nitropyridineHCID 253123—
Solvent1-ButanolHCID 263—
Product1-Boc-4-(6-methyl-5-nitro-2-pyridinyl)-piperazineHCID 6853803799%

Reaction Conditions

Temperature30 °C

Reaction Steps

Mechanically stir mixture of 6-chloro-2-methyl-3-nitro-pyridine (Asymchem, 25.00 g, 144.9 mmol), tert-butyl 1-piperazinecarboxylate (29.68 g, 159.4 mmol), and triethylamine (23.2 mL, 167 mmol) in n-BuOH (250 mL) at 50° C. under nitrogen for 4 hours, at 65° C. for 2 hours, then at room temperature overnight. Add additional tert-butyl 1-piperazinecarboxylate (1.5 g), and heat the reaction at 65° C. for 4 hours. Cool the resulting slurry to 30° C. then add hexanes (75 mL). Cool the slurry to room temperature over 1 hour, then add water (150 mL). Allow the slurry to stand for 45 min then filter. Wash the cake with water (4×100 mL) then hexanes (100 mL) and air-dry overnight to yield 4-(6-methyl-5-nitro-pyridin-2-yl)-piperazine-1-carboxylic acid tert-butyl ester as bright yellow crystals (46.30 g, 99% yield, MS(ES): m/z=267 [M+H—C4H8]).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652015B2
Source datasetuspto-grants-2010_01
ORD IDord-1b5e40437390426ea79d40404430ecaa
Source noteuspto-grants-2010_01