Oxalyl chloride → 4-[[(2,4-Dimethylpyridin-3-yl)Carbonyl]Amino]-N-[[1-[4-(methylsulfonyl)Butyl]Cyclopentyl]Carbonyl]-L-Phenylalanine

To a solution of 2,4-dimethylpyridinecarboxylic acid (0.6 mmol, 102 mg) in dichloromethane (3 mL) was added a drop of DMF and oxalyl chloride (0.78 mmol, 99 mg) at 0° C. (ice bath). The solution was stirred at this temperature for 30 min, warmed to room temperature and stirred for an additional 1 h. Then, the solvent and excess oxalyl chloride was removed under vacuum and the residue was dried under high vacuum. To this 4-amino-N-[[1-[4-(methylsulfonyl)butyl]cyclopentyl]carbonyl]-L-phenylalanine methyl ester (0.5 mmol, 212 mg) was added and the mixture was dissolved in dichloromethane (5 mL). To this clear solution was added DIPEA (2.0 mmol, 0.258 g) at room temperature. The mixture was stirred for 15 h at which time TLC analysis of the mixture indicated the absence of starting material. Then, the mixture was diluted with dichloromethane (20 mL) and water (100 mL). The two layers were separated and the organic layer was washed with saturated sodium bicarbonate solution (20 mL), brine solution (30 mL) and dried over anhydrous magnesium sulfate. Filtration of the drying agent and removal of the solvent gave a crude product which was purified by silica gel column chromatography to afford 0.232 g (80%) of a white solid. HR MS (C29H39N3O6S): Obs. mass, 558.2629. Calcd. mass, 558.2638, M+H).

1. stirringstirred for an additional 1 h
2. customThen, the solvent and excess oxalyl chloride was removed under vacuum
3. customthe residue was dried under high vacuum
4. stirringThe mixture was stirred for 15 h at which time TLC analysis of the mixture
5. customThe two layers were separated
6. washthe organic layer was washed with saturated sodium bicarbonate solution (20 mL), brine solution (30 mL)
7. dry with materialdried over anhydrous magnesium sulfate
8. filtrationFiltration of the drying agent and removal of the solvent
9. customgave a crude product which
10. customwas purified by silica gel column chromatography

ORD-Eintrag

ord-fed86d3bec5e495cb1f257bc35a1d05d

Quelldatensatz

uspto-grants-2004_10

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US06806365B2