Hydrochloric Acid → HCID 58948143, Verbindung

Temperatur

0 °C

2,6-Dibromo-4-amino-5-nitro-pyridine (3 g) was taken up in concentrated hydrochloric acid (20 mL) and cooled to 0° C. Sodium nitrite (3.5 g) was added and the reaction mixture was allowed to stir at 0° C. for 1 h. The ice bath was removed and the reaction allowed to warm to room temperature over 3 h, and was then quenched by the addition of ethyl acetate (50 mL) and water (100 mL). The organic layer was separated, dried over MgSO4 and filtered and evaporated in vacuo to a pale yellow oil, which was purified by column chromatography using 35:1 pentane:EtOAc as eluant to give the title compound (2.2 g) as a white solid.

1. customThe ice bath was removed
2. temperatureto warm to room temperature over 3 h
3. customwas then quenched by the addition of ethyl acetate (50 mL) and water (100 mL)
4. customThe organic layer was separated
5. dry with materialdried over MgSO4
6. filtrationfiltered
7. customevaporated in vacuo to a pale yellow oil, which
8. customwas purified by column chromatography

ORD-Eintrag

ord-8f145f331fea473dbe193015c2f9acc9

Quelldatensatz

uspto-grants-2010_04

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US07691877B2