2-Amino-6-fluorobenzonitrile → N-(1-(3-amino-2-cyanophenoxy)-2-methylpropan-2-yl)cyclohexanecarboxamide
Reaction equation
[OH:1][CH2:2][C:3]([NH:6][C:7]([CH:9]1[CH2:14][CH2:13][CH2:12][CH2:11][CH2:10]1)=[O:8])([CH3:5])[CH3:4].[NH2:15][C:16]1[CH:23]=[CH:22][CH:21]=[C:20](F)[C:17]=1[C:18]#[N:19]>>[NH2:15][C:16]1[C:17]([C:18]#[N:19])=[C:20]([CH:21]=[CH:22][CH:23]=1)[O:1][CH2:2][C:3]([NH:6][C:7]([CH:9]1[CH2:14][CH2:13][CH2:12][CH2:11][CH2:10]1)=[O:8])([CH3:5])[CH3:4]Participants
3
Procedure
Prepared as in Example 22b from N-(1-hydroxy-2-methylpropan-2-yl)cyclohexanecarboxamide (Example 37c) and 2-amino-6-fluorobenzonitrile as an off-white solid (29%). MS 316 (MH+).
Sources & evidence
- ORD record
- ord-ad40a23117e94fffbb7bfcffa1ff744b
- Source dataset
- uspto-grants-2015_04
- Patent number
- US09000054B2
Reaction notes
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