Cyclopentanol → HCID 57968786, compound

HRID 1471533Notes

Reaction equation

HRID 1471533 reaction equation
[CH:1]1([OH:6])[CH2:5][CH2:4][CH2:3][CH2:2]1.[H-].[Na+].Cl[C:10]1[N:18]=[C:17]([Cl:19])[CH:16]=[CH:15][C:11]=1[C:12]([NH2:14])=[O:13]>CN(C=O)C>[Cl:19][C:17]1[CH:16]=[CH:15][C:11]([C:12]([NH2:14])=[O:13])=[C:10]([O:6][CH:1]2[CH2:5][CH2:4][CH2:3][CH2:2]2)[N:18]=1

Participants

5

Procedure

To a solution of cyclopentanol (1.42 mL, 15.70 mmol) in DMF (5 mL) at 0° C. was added sodium hydride (95% in mineral oil, 0.39 g, 15.70 mmol) in portions and stirred for 1 h at room temperature. This mixture was slowly added to a solution of 2,6-dichloro-nicotinamide (2.0 g, 10.47 mmol) in DMF (10 mL) at 0° C. The reaction mixture was stirred at room temperature overnight. DMF was removed under reduced pressure, and the resulting mixture was diluted with EtOAc (100 mL), washed with water (2×25 mL) and brine (2×25 mL) solution, dried over anhyd. Na2SO4, filtered, and concentrated to give yellow oil, which was purified by flash chromatography on silica gel using 10-25% EtOAc/hexanes as eluent to yield the title compound (1.94 g, 51%) as a transparent oil. 1H NMR (400 MHz, CDCl3) δ 8.44 (d, J=7.8 Hz, 1 H), 7.65 (br. s., 1 H), 7.03 (d, J=8.2 Hz, 1 H), 5.74 (br. s., 1 H), 5.70-5.57 (m, 1 H), 2.25-1.95 (m, 2 H), 1.90-1.66 (m, 6 H).

Workup

  1. stirringThe reaction mixture was stirred at room temperature overnight
  2. customDMF was removed under reduced pressure
  3. additionthe resulting mixture was diluted with EtOAc (100 mL)
  4. washwashed with water (2×25 mL) and brine (2×25 mL) solution
  5. customdried over anhyd
  6. filtrationNa2SO4, filtered
  7. concentrationconcentrated
  8. customto give yellow oil, which
  9. customwas purified by flash chromatography on silica gel using 10-25% EtOAc/hexanes as eluent

Sources & evidence

ORD record
ord-7145f2421ec74fb7a6be6dbb64c8ca6c
Source dataset
uspto-grants-2015_04
Patent number
US09012431B2

Reaction notes

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