5-Fluoroindole → 5-fluoro-3-(piperidin-4-yl)-1H-indole
Reaction equation
[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][CH:6]=[CH:5]2.Cl.O.[NH:13]1[CH2:18][CH2:17][C:16](=O)[CH2:15][CH2:14]1>>[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][CH:6]=[C:5]2[CH:16]1[CH2:17][CH2:18][NH:13][CH2:14][CH2:15]1Participants
3
Procedure
This compound was prepared following the procedure described in Example 1 (parts A and B) starting with 0.7 g (5.5 mmol) of 5-fluoroindol and 2.1 g (13.6 mmol) of 4-piperidone monohydrate hydrochloride. After the usual work-up 0.8 g (67% of yield) of the desired product were obtained.
Workup
- customThis compound was prepared
Sources & evidence
- ORD record
- ord-fe0eeb1995d145d5a9e718020c68c484
- Source dataset
- uspto-grants-2004_01
- Patent number
- US06683096B2
Reaction notes
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