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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627697Generated: October 26, 2026

2-Amino-5-chloropyridine → methyl 3-(5-chloro-2-iminopyridin-1(2H)-yl)-2-oxobutanoate hydrobromide

https://huagongshe.com/reaction/627697

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-chloropyridineHCID 66174—
ReactantMethyl 3-bromo-2-oxobutanoateHCID 11183175—
Solvent1,2-DimethoxyethaneHCID 8071—
Productmethyl 3-(5-chloro-2-iminopyridin-1(2H)-yl)-2-oxobutanoate hydrobromideHCID 8672814862%

Reaction Steps

To a solution of methyl 3-bromo-2-oxobutanoate (8.26 g, 42.4 mmol) in DME (33 mL) at room temperature was added 2-amino-5-chloropyridine (5.45 g, 42.4 mmol). The reaction mixture was stirred at room temperature for 20 h. The solid was collected by filtration, washed with EtOAc (2×), and dried under high vacuum to give methyl 3-(5-chloro-2-iminopyridin-1(2H)-yl)-2-oxobutanoate hydrobromide (8.51 g, 26.3 mmol, 62% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309263B2
Source datasetuspto-grants-2016_04
ORD IDord-c20f4f2d535545609f935574bdec11e5
Source noteuspto-grants-2016_04