2-Bromopyridine → HCID 15554650, compound

To a flask were added 3.2 g of 2-amino-6-methylpyridine, 4.9 g of 2-bromopyridine, 3.5 g of sodium tert-butoxide, and 120 ml toluene. The mixture was purged thoroughly with nitrogen and 83 mg of 1,1′-bis(diphenylphosphino)ferrocene and 34 mg of palladium acetate were added. The reaction mixture was heated to 65 C for 3 hours, to 75 C for 2 hours, and then cooled to 22 C. After quenching with 75 ml of water, the product was extracted with 75 ml ethyl acetate. The product was extracted with 50 ml of 1M hydrochloric acid, and washed with 30 ml of ethyl acetate. After basifying with 3M sodium hydroxide, the product was extracted with 75 ml of ethyl acetate and washed with 30 ml of water. Following solvent removal, the product was purified by silica gel chromatography using 38% ethyl acetate, 50% hexane, and 12% methanol resulting in an orange oil.

1. customThe mixture was purged thoroughly with nitrogen and 83 mg of 1,1′-bis(diphenylphosphino)ferrocene and 34 mg of palladium acetate
2. additionwere added
3. temperatureThe reaction mixture was heated to 65 C for 3 hours, to 75 C for 2 hours
4. temperaturecooled to 22 C
5. customAfter quenching with 75 ml of water
6. extractionthe product was extracted with 75 ml ethyl acetate
7. extractionThe product was extracted with 50 ml of 1M hydrochloric acid
8. washwashed with 30 ml of ethyl acetate
9. extractionthe product was extracted with 75 ml of ethyl acetate
10. washwashed with 30 ml of water
11. customFollowing solvent removal
12. customthe product was purified by silica gel chromatography

ORD record

ord-b53a03b0c6264240b33a32e519a913b5

Source dataset

uspto-grants-2015_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US09011734B2