2-Bromoethanol → HCID 10247304, compound

HRID 1534504Notes

Reaction equation

HRID 1534504 reaction equation
[C:1]([C:5]1[CH:6]=[N:7][C:8]2[C:13]([C:14]=1[NH:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=1[CH3:22])=[CH:12][CH:11]=[CH:10][C:9]=2[OH:23])(=[O:4])[CH2:2][CH3:3].[CH3:24][C:25](C)([O-:27])C.[K+].BrCCO>COCCOCCOC>[C:1]([C:5]1[CH:6]=[N:7][C:8]2[C:13]([C:14]=1[NH:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=1[CH3:22])=[CH:12][CH:11]=[CH:10][C:9]=2[O:23][CH2:24][CH2:25][OH:27])(=[O:4])[CH2:2][CH3:3]

Participants

5

Procedure

A solution of 3-propanoyl-4-(2-methylphenylamino)-8-hydroxyquinoline (3.06 g, 10 mmol) and potassium t-butoxide (1.68 g, 15 mmol) in diglyme (50 ml) was heated to 150°, a solution of 2-bromoethanol (0.85 ml, 12 mmol) in diglyme (25 ml) added dropwise, then the mixture raised to reflux temperature with vigorous stirring. After 1 hour a further portion of 2-bromoethanol (0.85 ml) was added, and reflux continued for 2 hours. The diglyme was evaporated, the residue taken up in dichloromethane, washed with water and brine, dried and evaporated. Chromatography (silica gel, ethyl acetate/2% acetic acid/2%-5% methanol) and recrystallization from aqueous isobutyl alcohol gave 3-propanoyl-4-(2-methylphenylamino)-8-(2-hydroxyethoxy)-quinoline (0.48 g), m.p. 174°-176°.

Workup

  1. temperaturethe mixture raised
  2. temperatureto reflux temperature with vigorous stirring
  3. temperaturereflux
  4. customThe diglyme was evaporated
  5. washwashed with water and brine
  6. customdried
  7. customevaporated
  8. customChromatography (silica gel, ethyl acetate/2% acetic acid/2%-5% methanol) and recrystallization from aqueous isobutyl alcohol

Sources & evidence

ORD record
ord-501aec6211fa42a2b7ed4c6f1f4d0007
Source dataset
uspto-grants-1992_02
Patent number
US05089504

Reaction notes

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