Pyridine → HCID 16749201, compound

HRID 2084458Notes

Reaction equation

HRID 2084458 reaction equation
[NH2:1]/[C:2](=[N:13]\[O:14][C:15]([C@H:17]([CH2:26][CH2:27][CH2:28][CH:29]1[CH2:34][CH2:33][CH2:32][CH2:31][CH2:30]1)[CH2:18][C:19]([O:21][C:22]([CH3:25])([CH3:24])[CH3:23])=[O:20])=O)/[CH:3]1[CH2:8][CH2:7][N:6]([S:9]([CH3:12])(=[O:11])=[O:10])[CH2:5][CH2:4]1.N1C=CC=CC=1>C1(C)C=CC=CC=1.CCOC(C)=O.[Cl-].[Cl-].[Zn+2]>[CH:29]1([CH2:28][CH2:27][CH2:26][C@@H:17]([C:15]2[O:14][N:13]=[C:2]([CH:3]3[CH2:8][CH2:7][N:6]([S:9]([CH3:12])(=[O:11])=[O:10])[CH2:5][CH2:4]3)[N:1]=2)[CH2:18][C:19]([O:21][C:22]([CH3:25])([CH3:24])[CH3:23])=[O:20])[CH2:34][CH2:33][CH2:32][CH2:31][CH2:30]1

Participants

6

Procedure

A solution of tert-butyl (3R)-3-{[({(Z)-amino[1-(methylsulfonyl)-4-piperidinyl]methylidene}amino)oxy]carbonyl}-6-cyclohexylhexanoate (preparation 42) (1.50 g, 1.83 mmol) in toluene (100 ml) was treated with pyridine (90 μl, 1.83 mmol) and anhydrous ZnCl2 (150 mg, 1.83 mmol) and heated at reflux for 20 hours. The reaction mixture was diluted with EtOAc and washed with H2O, brine and H2O, dried over anhydrous Na2SO4 and filtered. The solvent was removed under reduced pressure. The residue was purified on a silica column eluting with a solvent gradient of cyclohexane:EtOAc (90:10) gradually changing to (50:50). The oil was recrystallised from pentane to afford the title compound as a white solid (320 mg, 36%).

Workup

  1. temperatureheated
  2. temperatureat reflux for 20 hours
  3. washwashed with H2O, brine and H2O
  4. dry with materialdried over anhydrous Na2SO4
  5. filtrationfiltered
  6. customThe solvent was removed under reduced pressure
  7. customThe residue was purified on a silica column
  8. washeluting with a solvent gradient of cyclohexane:EtOAc (90:10)
  9. customThe oil was recrystallised from pentane

Sources & evidence

ORD record
ord-e9be7da3223844e6962a3975f7354a1f
Source dataset
uspto-grants-2004_04
Patent number
US06716861B2

Reaction notes

Loading…