Hydrochloric Acid → 2-(2-Iodophenyl)butanamide

HOBt (325 mg, 2.40 mmol), EDCl.HCl (461 mg, 2.40 mmol) and DIPEA (1.40 mL, 8.02 mmol) were added to a stirred solution of 2-(2-iodophenyl)butanoic acid (I1) (465 mg, 1.60 mmol) in dry THF (6 mL) and dry DMF (1 mL) under an atmosphere of nitrogen. After 10 minutes ammonium carbonate (770 mg, 8.02 mmol) was added in one portion and the resulting mixture stirred at room temperature for 24 hours. The volatiles were removed in vacuo and EtOAc (50 mL) and saturated aqueous NaHCO3 (50 mL) were added to the residue. The aqueous phase was extracted with EtOAc (2×50 mL), then the combined organic extracts were washed with brine and dried over MgSO4. The solvent was removed under reduced pressure and the resulting solid was purified by silica gel column chromatography (Biotage Isolera, SiO2 cartridge, 0-50% EtOAc in petroleum benzine 40-60° C.) to give the title compound I2 as a white solid (398 mg, 86%); NMR (400 MHz, d6-DMSO) δ 7.85 (dd, J=7.9, 1.2 Hz, 1H), 7.46 (dd, J=7.8, 1.7 Hz, 1H), 7.39 (s, 1H), 7.35 (td, J=7.6, 1.2 Hz, 1H), 7.02-6.92 (m, 2H), 3.59 (dd, J=8.8, 6.0 Hz, 1H), 1.92-1.78 (m, 1H), 1.65-1.51 (m, 1H), 0.86 (t, J=7.3 Hz, 3H). LCMS-A: rt 5.463 min; m/z 290 [M+H]+.

1. customThe volatiles were removed in vacuo and EtOAc (50 mL) and saturated aqueous NaHCO3 (50 mL)
2. additionwere added to the residue
3. extractionThe aqueous phase was extracted with EtOAc (2×50 mL)
4. washthe combined organic extracts were washed with brine
5. dry with materialdried over MgSO4
6. customThe solvent was removed under reduced pressure
7. customthe resulting solid was purified by silica gel column chromatography (Biotage Isolera, SiO2 cartridge, 0-50% EtOAc in petroleum benzine 40-60° C.)

ORD record

ord-7599411f68404a189b2756436ec962f7

Source dataset

uspto-grants-2016_01

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US09238644B2