Ethylene Glycol → HCID 57559134, compound

HRID 736098Notes

Reaction equation

HRID 736098 reaction equation
[CH2:1]([O:3][C:4]([C:6]1[C:12]2[NH:13][C:14]3[CH:15]=[CH:16][CH:17]=[CH:18][C:19]=3[C:11]=2[C:10](=[O:20])[CH2:9][N:8]([C:21](=[O:29])[C:22]2[CH:27]=[CH:26][C:25]([F:28])=[CH:24][CH:23]=2)[CH:7]=1)=[O:5])[CH3:2].CC1C=CC(S(O)(=O)=O)=CC=1.[CH2:41](O)[CH2:42][OH:43]>C1(C)C=CC=CC=1.C(Cl)Cl>[CH2:1]([O:3][C:4]([C:6]1[C:12]2[NH:13][C:14]3[CH:15]=[CH:16][CH:17]=[CH:18][C:19]=3[C:11]=2[C:10]2([O:43][CH2:42][CH2:41][O:20]2)[CH2:9][N:8]([C:21](=[O:29])[C:22]2[CH:27]=[CH:26][C:25]([F:28])=[CH:24][CH:23]=2)[CH:7]=1)=[O:5])[CH3:2]

Participants

6

Reactant 3

HCID 174Ethylene GlycolHCID 6101p-Toluenesulfonic acidHCID 57559126HCID 57559126, compound

Product 1

HCID 57559134HCID 57559134, compound

Reagents, catalysts & solvents 2

HCID 1140TolueneSolventHCID 6344DichloromethaneSolvent

Procedure

A mixture of 3-(4-fluorobenzoyl)-1-oxo-1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carboxylic acid ethyl ester (39 mg, 10.1 mmol) and TsOH (10 mg) and ethylene glycol (0.2 mL) in toluene (10 mL) was heated to reflux overnight under nitrogen. After cooling, the reaction was diluted with DCM. It was then washed with saturated aqueous NaHCO3 and water and dried over MgSO4. Evaporation of solvent gave a crude product, which was purified by column chromatography on silica gel eluted with MeOH-DCM (2:98) to give the title compound (7.5 mg); 1H-NMR (CDCl3): δ 9.68 (1H, s), 8.24 (1H, d), 7.08 (2H, m), 7.57 (1H, s), 7.41 (2H, m), 7.12 (2H, m), 4.77 (2H, m), 4.55 (2H, m), 4.46 (2H, q), 1.46 (3H, t). MS (ES): 437 (MH+).

Workup

  1. temperaturewas heated
  2. temperatureto reflux overnight under nitrogen
  3. temperatureAfter cooling
  4. washIt was then washed with saturated aqueous NaHCO3 and water
  5. dry with materialdried over MgSO4
  6. customEvaporation of solvent
  7. customgave a crude product, which
  8. customwas purified by column chromatography on silica gel
  9. washeluted with MeOH-DCM (2:98)

Sources & evidence

ORD record
ord-91e615549a6b4fe6a3a6e070f07d7ca3
Source dataset
uspto-grants-2009_09
Patent number
US07595311B2

Reaction notes

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