Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471288Generated: October 26, 2026

2-Bromo-6-methylpyridine → 2-methyl-N-(6-methylpyridin-2-yl)quinolin-8-amine

https://huagongshe.com/reaction/1471288

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-6-methylpyridineHCID 79205—
Reactant2-Methyl-8-aminoquinolineHCID 140457—
ReactantSodium t-butoxideHCID 23676156—
SolventTolueneHCID 1140—
Product2-methyl-N-(6-methylpyridin-2-yl)quinolin-8-amineHCID 6662783668%

Reaction Steps

To a flask were added 4.2 g of 2-methylquinolin-8-amine, 4.6 g of 6-methyl-2-bromopyridine, 3.3 g of sodium tert-butoxide, and 75 ml toluene. The mixture was purged thoroughly with nitrogen and 44 mg of 1,1′-bis(diphenylphosphino)ferrocene and 18 mg of palladium acetate were added. The reaction mixture was heated to 80 C for 16 hours, and then cooled to 22 C. After quenching with 100 ml of water, the product was extracted with 75 ml ethyl acetate. The product was extracted with 120 ml of 1M hydrochloric acid, and then basified with 3M sodium hydroxide. Following extraction with 75 ml of ethyl acetate and washing with 30 ml of water, the solvent was removed. The product was purified by dissolving in a hot mixture of 20 ml of 2-propanol and 5 ml of water, and after cooling to 5 C, the product was filtered, washed with 50% 2-propanol, and dried, resulting in 4.5 g of a tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09011734B2
Source datasetuspto-grants-2015_04
ORD IDord-c4be5fa5045f459897bd93b0d6bf4215
Source noteuspto-grants-2015_04