Methyl iodide → HCID 69415500, compound
Reaction equation
[C:1](=O)([O-])[O-].[K+].[K+].[CH3:7][O:8][C:9]([C:11]1[S:12][CH:13]=[CH:14][C:15]=1[S:16](=[O:28])(=[O:27])[NH:17][CH2:18][CH2:19][C:20]1[CH:25]=[CH:24][C:23]([F:26])=[CH:22][CH:21]=1)=[O:10].CI>>[CH3:7][O:8][C:9]([C:11]1[S:12][CH:13]=[CH:14][C:15]=1[S:16](=[O:27])(=[O:28])[N:17]([CH2:18][CH2:19][C:20]1[CH:21]=[CH:22][C:23]([F:26])=[CH:24][CH:25]=1)[CH3:1])=[O:10]Participants
4
Procedure
In the presence of potassium carbonate (2.58 g), 3-[2-(4-fluorophenyl)-ethylsulfamoyl]-thiophene-2-carboxylic acid methylester (3.2 g) was reacted with methyl iodide (0.69 mL), and an oily substance (3.38 g) was obtained, in the same way as Preparation Example 52.
Workup
- customan oily substance (3.38 g) was obtained, in the same way as Preparation Example 52
Sources & evidence
- ORD record
- ord-6fe10a1b34b14e6b9a03a2907b3fcba7
- Source dataset
- uspto-grants-2007_05
- Patent number
- US07217723B2
Reaction notes
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