4-(5-Fluoro-1H-indol-3-YL)cyclohexanone → 4-(6-Fluoro-1H-indol-3-YL)cyclohexanone
Reaction equation
FC1C=C2C(=CC=1)NC=C2C1CCC(=O)CC1.C1O[C:21]2([CH2:26][CH2:25][CH:24]([C:27]3[C:35]4[C:30](=[CH:31][C:32]([F:36])=[CH:33][CH:34]=4)[NH:29][CH:28]=3)[CH2:23][CH2:22]2)[O:20]C1>>[F:36][C:32]1[CH:31]=[C:30]2[C:35]([C:27]([CH:24]3[CH2:23][CH2:22][C:21](=[O:20])[CH2:26][CH2:25]3)=[CH:28][NH:29]2)=[CH:34][CH:33]=1Participants
3
Procedure
This compound was prepared in the manner as described above for (3a) by replacing 4-(5-fluoro-1H-3-indolyl)-cyclohexanone ethylene ketal with 4-(6-fluoro-1H-3-indolyl)-cyclohexanone ethylene ketal (5.4 g) in 99% (19.3 g) yield as a white solid: mp 102-105° C.
Workup
- customThis compound was prepared in the manner
- customyield as a white solid
Sources & evidence
- ORD record
- ord-5c78478023674d2397a473ce0806585d
- Source dataset
- uspto-grants-2000_08
- Patent number
- US06110956
Reaction notes
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