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Methanesulfonic Acid → HCID 25195527, compound

HRID 1436944
Notes
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Reaction equation

HRID 1436944 reaction equation
[NH2:1][C@@H:2]([CH2:6][O:7][C:8]([O:10][C:11]1[C:16]([CH:17]([CH3:19])[CH3:18])=[CH:15][CH:14]=[CH:13][C:12]=1[CH:20]([CH3:22])[CH3:21])=[O:9])[C:3]([OH:5])=[O:4].[CH3:23][S:24]([OH:27])(=[O:26])=[O:25]>O>[S:24]([OH:27])(=[O:26])(=[O:25])[CH3:23].[NH2:1][C@@H:2]([CH2:6][O:7][C:8]([O:10][C:11]1[C:16]([CH:17]([CH3:18])[CH3:19])=[CH:15][CH:14]=[CH:13][C:12]=1[CH:20]([CH3:22])[CH3:21])=[O:9])[C:3]([OH:5])=[O:4]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 6395Methanesulfonic AcidHCID 11716529HCID 11716529, compound

Product 1

HCID 25195527HCID 25195527, compound

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

To a suspension of compound (3) (4.44 g, 14.3 mmol) in H2O (100 mL) was added methanesulfonic acid (0.93 mL, 14.3 mmol). The resulting mixture was stirred at room temperature until the solid had completely dissolved. The solution was then frozen and lyophilized to afford the desired product as a light pinkish solid.

Workup

  • dissolutionhad completely dissolved
  • temperatureThe solution was then frozen
  • Sources & evidence

    ORD record
    ord-db21fdc496b54fceaadb8634386f1e02
    Source dataset
    uspto-grants-2009_11
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US07619110B2

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes