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Methanesulfonic Acid → HCID 25195527, compound

HRID 563052
Notes
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Reaction equation

HRID 563052 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-4ff5210a100244faafa6b131919b4b2c
    Source dataset
    uspto-grants-2011_11
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US08067455B2

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes