Diethyl Ether → 5-Ethynylpyridin-2-amine

2-Amino-5-bromopyridine (8.65 g, 50.0 mmole) and bis-trimethyl-silylacetamide (36.76 mL, 150.0 mmole) was stirred at 100° C. overnight. The mixture was purified by distillation to give 10.41 g (85%) of the protected amine. 2-Trimethylsilylamlno-5-bromopyridine (4.90 g, 20.0 mmole), bis(triphenylphosphine)palladium-(II) chloride (0.70 g, 1.00 mmole) and trimethylsilylacetylene (5.65 mL, 40.0 mmole) in piperidine (2 mL) was stirred under nitrogen at 80° C. overnight. Diethyl ether and NH4Cl (aq) was added to the mixture and the organic phase was separated, dried over Na2SO4 and evaporated. Tetrabutylammonium chloride (50.0 mL, 100.0 mmole) and THF (250 mL) was added to remove the protection groups and the mixture was stirred overnight. THF was evaporated. The residue was purified by silica gel column chromatography (EtOAc/Hexane, 40:60) to give 2.36 g, (61%) of the titled compound. 1H NMR (250 MHz, CDCl3) δ 3.05 (s, 1H), 4.65 (br s, 2H), 6.45 (d, 1H), 7.50 (dd, 1H), 8.25 (d, 1H).

1. customthe organic phase was separated
2. dry with materialdried over Na2SO4
3. customevaporated
4. customto remove the protection groups
5. customTHF was evaporated
6. customThe residue was purified by silica gel column chromatography (EtOAc/Hexane, 40:60)

ORD record

ord-930a834ddbcd4a67b71dd0a260357c2a

Source dataset

uspto-grants-2002_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06376492B1