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Propionic Acid → 2-Ethylthiazolo[4,5-c]quinoline

HRID 857976
Notes
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Reaction equation

HRID 857976 reaction equation
[NH2:1][C:2]1[CH:3]=[N:4][C:5]2[C:10]([C:11]=1[SH:12])=[CH:9][CH:8]=[CH:7][CH:6]=2.[C:13](O)(=O)[CH2:14][CH3:15]>>[CH2:14]([C:15]1[S:12][C:11]2[C:10]3[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=3[N:4]=[CH:3][C:2]=2[N:1]=1)[CH3:13]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 1032Propionic AcidHCID 1785079903-Aminoquinoline-4-thiol

Product 1

HCID 150279042-Ethylthiazolo[4,5-c]quinoline

Procedure

Propionyl anhydride (20 mL) was added to a suspension of 3-amino-quinoline-4-thiol (15 g) in propionic acid (100 mL). The reaction mixture was heated at reflux overnight and then filtered to remove a precipitate. The filtrate was concentrated under vacuum. The residue was taken up in dichloromethane (200 mL), washed with sodium bicarbonate then with water, and then dried over magnesium sulfate. The solution was filtered through a layer of silica gel eluting first with 1:1 ethyl acetate:hexane and then with ethyl acetate. The filtrate was evaporated to provide 2.6 g of 2-ethylthiazolo[4,5-c]quinoline as a yellow oil.

Workup

  1. temperatureThe reaction mixture was heated
  2. temperatureat reflux overnight
  3. filtrationfiltered
custom
to remove a precipitate
  • concentrationThe filtrate was concentrated under vacuum
  • washwashed with sodium bicarbonate
  • dry with materialwith water, and then dried over magnesium sulfate
  • filtrationThe solution was filtered through a layer of silica gel eluting first with 1:1 ethyl acetate
  • customThe filtrate was evaporated
  • Sources & evidence

    ORD record
    ord-51fa8a56c1a94deaa363baa89592238b
    Source dataset
    uspto-grants-2006_12
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US07148232B2

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes