HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Ethanol → 4-[[4-(3-chlorophenyl)-1,2-dihydro-2-oxo-6-quinolinyl]ethoxy(1-methyl-1H-imidazol-5-yl)methyl]benzaldehyde oxime

HRID 346986
Notes
Print preview

Reaction equation

HRID 346986 reaction equation
Cl.[NH2:2][OH:3].Cl.[Cl:5][C:6]1[CH:7]=[C:8]([C:12]2[C:21]3[C:16](=[CH:17][CH:18]=[C:19]([C:22]([OH:37])([C:31]4[N:35]([CH3:36])[CH:34]=[N:33][CH:32]=4)[C:23]4[CH:30]=[CH:29][C:26]([CH:27]=O)=[CH:25][CH:24]=4)[CH:20]=3)[NH:15][C:14](=[O:38])[CH:13]=2)[CH:9]=[CH:10][CH:11]=1.C([O-])([O-])=O.[K+].[K+].[CH2:45](O)[CH3:46]>>[Cl:5][C:6]1[CH:7]=[C:8]([C:12]2[C:21]3[C:16](=[CH:17][CH:18]=[C:19]([C:22]([O:37][CH2:45][CH3:46])([C:31]4[N:35]([CH3:36])[CH:34]=[N:33][CH:32]=4)[C:23]4[CH:30]=[CH:29][C:26]([CH:27]=[N:2][OH:3])=[CH:25][CH:24]=4)[CH:20]=3)[NH:15][C:14](=[O:38])[CH:13]=2)[CH:9]=[CH:10][CH:11]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 4

HCID 702EthanolHCID 11430Potassium CarbonateHCID 443297Hydroxyamine hydrochlorideHCID 21082104(+/-)-4-[[4-(3-chlorophenyl)-1,2-dihydro-2-oxo-6-quinolinyl]hydroxy(1-methyl-1H-imidazol-5-yl)methyl]benzaldehyde monohydrochloride

Product 1

HCID 867603784-[[4-(3-chlorophenyl)-1,2-dihydro-2-oxo-6-quinolinyl]ethoxy(1-methyl-1H-imidazol-5-yl)methyl]benzaldehyde oxime

Procedure

Hydroxylamine, hydrochloride (0.0131 mol) was added to a solution of (±)-4-[[4-(3-chlorophenyl)-1,2-dihydro-2-oxo-6-quinolinyl]hydroxy(1-methyl-1H-imidazol-5-yl)methyl]benzaldehyde monohydrochloride (described in Example B1) (0.0087 mol) in ethanol (45 ml). The mixture was stirred at room temperature for 1 hour and 30 minutes then refluxed for 2 hours, poured out into K2CO3 10% and extracted with EtOAc. The organic layer was separated, dried MgSO4), filtered and the solvent was evaporated. The residue (4.86 g) was purified by column chromatography over silica gel (eluent: CH2Cl2/CH3OH/NH4OH 95/5/0.1; 15–40 μm). The pure fractions were collected and the solvent was evaporated, yielding: two fractions. The first fraction was crystallized from CH3CN/diethyl ether. The precipitate was filtered off and dried, yielding 1.69 g (38%) of -4-[[4-(3-chlorophenyl)-1,2-dihydro-2-oxo-6-quinolinyl]ethoxy(1-methyl-1H-imidazol-5-yl)methyl]benzaldehyde oxime, of indeterminate E/Z configuration mp. 232° C. The second fraction was crystallized from CH3CN/diethyl ether. The precipitate was filtered off and dried, yielding 1.91 g (45%) of -4-[[4-(3-chlorophenyl)-1,2-dihydro-2-oxo-6-quinolinyl]hydroxy(1-methyl-1H-imidazol-5-yl)methyl]benzaldehyde oxime, of indeterminate E/Z configuration, mp. 230° C.

Workup

  1. temperaturethen refluxed for 2 hours
  2. extractionextracted with EtOAc
  3. customThe organic layer was separated
  4. filtrationdried MgSO4), filtered
  5. customthe solvent was evaporated
  6. customThe residue (4.86 g) was purified by column chromatography over silica gel (eluent: CH2Cl2/CH3OH/NH4OH 95/5/0.1; 15–40 μm)
  7. customThe pure fractions were collected
  8. customthe solvent was evaporated
  9. customyielding
  10. customThe first fraction was crystallized from CH3CN/diethyl ether
  11. filtrationThe precipitate was filtered off
  12. customdried

Sources & evidence

ORD record
ord-9f508ccf373141a3b814f1e753c4496a
Source dataset
uspto-grants-2007_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07173040B2

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes