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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640419Generated: October 31, 2026

Methanol → 2-(Methylamino)-2-oxoethyl 4-(6-bromo-3-pyridyl)-1-piperazinecarboxylate

https://huagongshe.com/reaction/1640419

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantMethylamineHCID 6329—
ReactantDichloromethaneHCID 6344—
ReactantHCID 60209561HCID 60209561—
SolventTetrahydrofuranHCID 8028—
Product2-(Methylamino)-2-oxoethyl 4-(6-bromo-3-pyridyl)-1-piperazinecarboxylateHCID 60209563—

Reaction Steps

The procedure described in Example 1 (step 1.4.) is used. Starting with 2.35 g (6.32 mmol) of 2-(ethyloxy)-2-oxoethyl 4-(6-bromo-3-pyridyl)-1-piperazinecarboxylate, obtained in step 7.4. of Example 7, and 15.80 ml (31.61 mmol) of a solution of methylamine (2M) in tetrahydrofuran, and after chromatography on silica gel, eluting with a 98/2 and then 97/3 mixture of dichloromethane and methanol, 1.779 g of product are obtained in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114866B2
Source datasetuspto-grants-2012_02
ORD IDord-56f47581540645c5a26554af2753aa36
Source noteuspto-grants-2012_02