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Thionyl Chloride → Methyl 4-chlorocinnoline-3-carboxylate

HRID 1178245
Notes
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Reaction equation

HRID 1178245 reaction equation
S(Cl)([Cl:3])=O.O[C:6]1[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[N:9]=[N:8][C:7]=1[C:16]([O:18][CH3:19])=[O:17]>>[Cl:3][C:6]1[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[N:9]=[N:8][C:7]=1[C:16]([O:18][CH3:19])=[O:17]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 24386Thionyl ChlorideHCID 178499158HCID 178499158, compound

Product 1

HCID 20187472Methyl 4-chlorocinnoline-3-carboxylate

Procedure

Thionyl chloride (8.15 g, 5 ml) was added dropwise under inert atmosphere to methyl 4-hydroxycinnoline-3-carboxylate (0.50 g, 2.45 mmol). The mixture was heated to reflux for 1.5 h, cooled to room temperature and excess thionyl chloride was removed under vacuum. Toluene (5 ml) was added to the residue. The mixture was stirred at room temperature overnight. The solids were collected by filtration and dried under vacuum. The title compound was isolated as a brown solid (248 mg, 1.11 mmol, 45%). LCMS: m/z 223 [M+H]+.

Workup

  1. temperatureThe mixture was heated
  2. temperatureto reflux for 1.5 h
  3. customexcess thionyl chloride was removed under vacuum
  4. additionToluene (5 ml) was added to the residue
  • filtrationThe solids were collected by filtration
  • customdried under vacuum
  • Sources & evidence

    ORD record
    ord-f7d5d4fe378f445ba79dd47106785524
    Source dataset
    uspto-grants-2007_10
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US07276505B2

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes