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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437355Generated: October 30, 2026

Chlorosuccinimide → Methyl 6-amino-5-bromo-3-chloropyridine-2-carboxylate

https://huagongshe.com/reaction/1437355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantMethyl 6-amino-5-bromopicolinateHCID 10704661—
SolventAcetic AcidHCID 176—
ProductMethyl 6-amino-5-bromo-3-chloropyridine-2-carboxylateHCID 2187380795.5%

Reaction Steps

To a solution methyl 6-amino-5-bromopyridine-2-carboxylate (20.04 g) in acetic acid (900 ml) was added N-chlorosuccinimide (14 g) and the resultant solution was heated to 120° C. for 1 hour. The solution was then evaporated and treated with excess aqueous sodium bicarbonate and extracted with dichloromethane. The organic fraction was dried and evaporated to give the product (21.98 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622481B2
Source datasetuspto-grants-2009_11
ORD IDord-29fa8d81c271442092e54bbd5c074631
Source noteuspto-grants-2009_11