Methyl iodide → [2-(6-Chloro-1,2-dimethyl-1H-indol-3-ylsulfanyl)-phenyl]-acetic acid
Reaction equation
[Cl:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6]([S:12][C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=3[CH2:19][C:20]([OH:22])=[O:21])=[C:7]([CH3:11])[NH:8]2)=[CH:4][CH:3]=1.I[CH3:24]>>[Cl:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6]([S:12][C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=3[CH2:19][C:20]([OH:22])=[O:21])=[C:7]([CH3:11])[N:8]2[CH3:24])=[CH:4][CH:3]=1Participants
3
Procedure
Prepared according to the procedure described in Example 5, Step 2, using the following starting materials: [2-(6-chloro-2-methyl-1H-indol-3-ylsulfanyl)-phenyl]-acetic acid and iodomethane.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-912dc88065d94714a8908de825d93c6b
- Source dataset
- uspto-grants-2015_04
- Patent number
- US09000025B2
Reaction notes
Loading…