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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588363Generated: October 30, 2026

2-Chloro-5-methyl-3-nitropyridine → Ethyl 5-((5-methyl-3-nitropyridin-2-yl)amino)picolinate

https://huagongshe.com/reaction/588363

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-5-methyl-3-nitropyridineHCID 818300—
ReactantEthyl 5-aminopyridine-2-carboxylateHCID 13816714—
ProductEthyl 5-((5-methyl-3-nitropyridin-2-yl)amino)picolinateHCID 11765297953.4%

Reaction Steps

Prepared according to General Procedure E starting from ethyl 5-aminopicolinate (14.0 g, 84.2 mmol) and 2-chloro-5-methyl-3-nitropyridine (17.4 g, 101 mmol) to give the title compound as a yellow solid (13.6 g, 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227956B2
Source datasetuspto-grants-2016_01
ORD IDord-7e02379a946e45df80e56da4b1c97645
Source noteuspto-grants-2016_01