HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Bromo-2-methoxypyridine → HCID 13433420, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Bromo-2-methoxypyridine | HCID 2734895 | — |
| Reactant | 2-Bromo-5-(methylthio)pyridine | HCID 11658494 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13433420 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05593994 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-c1393a34c87c413eb89d69d24eafa025 |
| Source note | uspto-grants-1997_01 |