Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 233573Generated: October 25, 2026

5-Bromo-2-methoxypyridine → HCID 13433420, compound

https://huagongshe.com/reaction/233573

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-2-methoxypyridineHCID 2734895—
Reactant2-Bromo-5-(methylthio)pyridineHCID 11658494—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13433420HCID 13433420—

Reaction Steps

For example, 2-bromo-5-methylthiopyridine may be prepared by the treatment of 2-methoxy-5-bromopyridine (Shiao. M. J. et. al. Syn. Comm. 20(19), 2971, 1990) with n-butyllithium in anhydrous tetrahydrofuran at -78 ° C. followed by quenching the reaction with dimethyldisulfide to afford 2-methoxy-5-methylthiopyridine. Demethylation provides 2-hydroxy-5-methylthiopyridine which upon reaction with phosphorousoxybromide yields the desired 2-bromo-5-methylthiopyridine starting material. (Scheme 7) ##STR19##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05593994
Source datasetuspto-grants-1997_01
ORD IDord-c1393a34c87c413eb89d69d24eafa025
Source noteuspto-grants-1997_01