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Water → HCID 57680938, compound

HRID 493752
Notes
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Reaction equation

HRID 493752 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[CH3:12])[N:8]=[CH:7][CH:6]=[CH:5]2.[Li][C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1.O>C1COCC1>[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[CH3:12])[N:8]=[C:7]([C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1)[CH:6]=[CH:5]2
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 962WaterHCID 45253046-Chloro-7-methylquinolineHCID 178506676HCID 178506676, compound

Product 1

HCID 57680938HCID 57680938, compound

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Conditions

Temperature
0 °C

Procedure

Into a solution of 6-chloro-7-methylquinoline (1000 mg, 5.644 mmol) in THF (5 mL), which was cooled in ice/water bath under N2, was added PhLi (1.9 M in THF, 2.971 mL) dropwise over 5 min. After stirring at 0° C. for 15 min, the ice/water bath was removed and the reaction mixture was stirred at rt. After 4 h, MeOH (5 mL) was added to quench the reaction and the reaction mixture was stirred at rt overnight. After that time, the mixture was poured into water (20 mL) and extracted with EtOAc (3×30 mL). The organic extracts were dried over MgSO4, filtered, and concentrated in vacuo. The residue was dissolved in acetonitrile (30 mL) and DDQ (1282 mg) was added and the solution was stirred under N2 at rt for 24 h. After that time, the reaction mixture was poured into aqueous NaOH (3 N, 50 mL) and extracted with EtOAc (2×75 mL). The extracts were washed with aqueous NaOH (3N, 2×50 mL), water (2×50 mL) and brine (50 mL), dried over MgSO4, filtered, and concentrated in vacuo to afford the title compounds; 1H NMR (CDCl3, 400 MHz) δ 2.60 (s, 3H), 7.47-7.55 (m, 3H), 7.83-7.86 (m, 2H), 8.04 (s, 1H), 8.10-8.16 (m, 3H); MS(ES): 254.1/256.1 (M/M+2).

Workup

  1. customthe ice/water bath was removed
  2. stirringthe reaction mixture was stirred at rt
  3. waitAfter 4 h
  4. additionMeOH (5 mL) was added
  5. customto quench
  6. customthe reaction
  7. stirringthe reaction mixture was stirred at rt overnight
  8. extractionextracted with EtOAc (3×30 mL)
  9. dry with materialThe organic extracts were dried over MgSO4
  10. filtrationfiltered
  11. concentrationconcentrated in vacuo
  12. dissolutionThe residue was dissolved in acetonitrile (30 mL)
  13. additionDDQ (1282 mg) was added
  14. stirringthe solution was stirred under N2 at rt for 24 h
  15. additionAfter that time, the reaction mixture was poured into aqueous NaOH (3 N, 50 mL)
  16. extractionextracted with EtOAc (2×75 mL)
  17. washThe extracts were washed with aqueous NaOH (3N, 2×50 mL), water (2×50 mL) and brine (50 mL)
  18. dry with materialdried over MgSO4
  19. filtrationfiltered
  20. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-6917296dcedf4bbb9c783afd38bd52b1
Source dataset
uspto-grants-2009_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07534797B2

Reaction notes

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