2-Bromo-6-methylpyridine → HCID 52936008, compound

Participants

Reaction Conditions

Reaction Steps

To a solution of (2S,4R)-1-acetyl-6-[1-(2-{[(1,1-dimethylethyl)(dimethyl)silyl]oxy}ethyl)-1H-1,2,3-triazol-4-yl]-2-methyl-1,2,3,4-tetrahydro-4-quinolinamine (for a preparation, see Intermediate 44) (59 mg, 0.137 mmol) and 2-bromo-6-methylpyridine (70.9 mg, 0.412 mmol) in toluene (2.5 mL) were successively added sodium tert-butoxide (132 mg, 1.373 mmol), tris(dibenzylideneacetone)dipalladium(0) (25.2 mg, 0.027 mmol) and 2′-(dicyclohexylphosphino)-N,N-dimethylbiphenyl-2-amine (DavePhos) (21.62 mg, 0.055 mmol). The reaction mixture was stirred at 75° C. for 5 h then cooled to room temperature and filtered through Celite. The insoluble material was washed with 5% MeOH in DCM and the combined filtrate and washings were concentrated in vacuo. The residue was dissolved in a 1:1 MeOH/DMSO mixture and was purified by MDAP (modifier: formic acid). The appropriate fractions were combined and the solvents evaporated using a blow down apparatus (nitrogen inlet) to give 2-(4-{(2S,4R)-1-acetyl-2-methyl-4-[(6-methyl-2-pyridinyl)amino]-1,2,3,4-tetrahydro-6-quinolinyl}-1H-1,2,3-triazol-1-yl)ethanol (12.5 mg, 0.031 mmol, 22%) as a viscous yellow oil.

Provenance & Evidence