2-Tetralone → HCID 66579857, compound
Reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[O:12][N:11]=[C:10]([CH3:13])[C:9]=2[NH2:14])=[CH:4][CH:3]=1.[CH2:15]1[C:24]2[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=2)[CH2:18][CH2:17][C:16]1=O>>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[O:12][N:11]=[C:10]([CH3:13])[C:9]=2[NH:14][CH:21]2[CH2:22][CH2:23][C:24]3[C:19](=[CH:18][CH:17]=[CH:16][CH:15]=3)[CH2:20]2)=[CH:6][CH:7]=1Participants
3
Procedure
Prepared according to the procedure described in Example 24, Step 1, using 5-(4-bromo-phenyl)-3-methyl-isoxazol-4-ylamine and 3,4-dihydro-1H-naphthalen-2-one.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-9a517186da4f49beba186a6aff025760
- Source dataset
- uspto-grants-2015_07
- Patent number
- US09090573B2
Reaction notes
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