3-Fluoroaniline → HCID 66624960, compound
Reaction equation
[C:1]([N:4]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[C@@H:7]([OH:14])[CH2:6][C@@H:5]1[CH3:15])(=[O:3])[CH3:2].[F:16][C:17]1[CH:18]=[C:19]([CH:21]=[CH:22][CH:23]=1)N>>[C:1]([N:4]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[C@H:7]([O:14][C:22]2[CH:21]=[CH:19][CH:18]=[C:17]([F:16])[CH:23]=2)[CH2:6][C@@H:5]1[CH3:15])(=[O:3])[CH3:2]Participants
3
Procedure
A compound was produced in the same manner as in Example 12, using 100 mg of trans-1-acetyl-4-hydroxy-2-methyl-1,2,3,4-tetrahydroquinoline and 112 mg of 3-fluoroaniline, and thus 70 mg (47%) of the title compound was obtained as a colorless oily substance.
Workup
- customA compound was produced in the same manner as in Example 12
Sources & evidence
- ORD record
- ord-d4e8acfa44314b94a94b9ede51665d58
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09045423B2
Reaction notes
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