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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1939245Generated: November 1, 2026

Chlorine → Methyl-6-amino-5-chloro-2-methoxypyridine-3-carboxylate

https://huagongshe.com/reaction/1939245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorineHCID 24526—
ReactantMethyl 6-amino-2-methoxynicotinateHCID 11159681—
SolventAcetic AcidHCID 176—
ProductMethyl-6-amino-5-chloro-2-methoxypyridine-3-carboxylateHCID 2210179867.3%

Reaction Steps

A solution of methyl-6-amino-2-methoxypyridine-3-carboxylate (0.4 g) in acetic acid (10 ml) was treated with a solution of Cl2 (0.19 g) in HOAc (4 ml) at room temperature for 3 h. The AcOH was removed by rotary evaporation and the residue treated with aqueous NaHCO3 (50 mL) and the product extracted into EtOAc (100 mL). Evaporation afforded methyl-6-amino-5-chloro-2-methoxypyridine-3-carboxylate (0.32 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05696129
Source datasetuspto-grants-1997_12
ORD IDord-8ee492bec8e14475aa6f0e1f353636af
Source noteuspto-grants-1997_12