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Methanol → HCID 31699716, compound

HRID 877651
Notes
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Reaction equation

HRID 877651 reaction equation
[CH3:1][N:2]1[CH2:7][CH2:6][N:5]([S:8]([C:11]2[CH:12]=[C:13]([CH:17]=[CH:18][CH:19]=2)[C:14]([OH:16])=[O:15])(=[O:10])=[O:9])[CH2:4][CH2:3]1.S(=O)(=O)(O)O.[CH3:25]O>>[CH3:1][N:2]1[CH2:7][CH2:6][N:5]([S:8]([C:11]2[CH:12]=[C:13]([CH:17]=[CH:18][CH:19]=2)[C:14]([O:16][CH3:25])=[O:15])(=[O:10])=[O:9])[CH2:4][CH2:3]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 887MethanolHCID 1118Sulfuric AcidHCID 10814563-[(4-Methylpiperazin-1-yl)sulfonyl]benzoic acid

Product 1

HCID 31699716HCID 31699716, compound

Procedure

3-((4-methylpiperazin-1-yl)sulfonyl)benzoic acid (250 mg, 0.879 mmol) was refluxed in the presence of concentrated sulfuric acid (5.68 mg, 0.044 mmol) in methanol at 70° C. for overnight. Reaction was monitored by TLC. After completion of the reaction, solvent was removed by vacuum and the crude material was used for further reaction without purification.

Workup

  1. customReaction
  2. customAfter completion of the reaction, solvent
  • customwas removed by vacuum
  • customthe crude material was used for further reaction without purification
  • Sources & evidence

    ORD record
    ord-e6a8ab16811f44fb9c9c6f9321fab7e5
    Source dataset
    uspto-grants-2015_03
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US08987335B2

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes