Potassium Carbonate → HCID 11702428, compound
Reaction equation
[CH3:1][S:2]([O:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([CH:12]2[CH2:17][CH2:16][NH:15][CH2:14][CH2:13]2)[C:7]=1[F:18])(=[O:4])=[O:3].C(=O)([O-])[O-].[K+].[K+].I[CH2:26][CH2:27][CH3:28]>C(#N)C>[CH3:1][S:2]([O:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([CH:12]2[CH2:13][CH2:14][N:15]([CH2:26][CH2:27][CH3:28])[CH2:16][CH2:17]2)[C:7]=1[F:18])(=[O:3])=[O:4]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Preparation according to Example 1: 2-fluoro-3-piperidin-4-ylphenyl methanesulfonate (0.01 g), acetonitrile (2 ml), potassium carbonate (0.01 g) and iodopropane (0.01 g). MS m/z (rel. intensity, 70 eV) 315 (M+, 4), 287 (16), 286 (bp), 236 (2), 207 (41).
Workup
- customPreparation
Sources & evidence
- ORD record
- ord-317c8076211f46d389a012c5de13c42d
- Source dataset
- uspto-grants-2012_11
- Patent number
- US08314126B2
Reaction notes
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