2-Amino-6-fluorobenzonitrile → N-(4-(3-amino-2-cyanophenoxy)cyclohexyl)isobutyramide
Reaction equation
[OH:1][CH:2]1[CH2:7][CH2:6][CH:5]([NH:8][C:9](=[O:13])[CH:10]([CH3:12])[CH3:11])[CH2:4][CH2:3]1.[NH2:14][C:15]1[CH:22]=[CH:21][CH:20]=[C:19](F)[C:16]=1[C:17]#[N:18]>>[NH2:14][C:15]1[C:16]([C:17]#[N:18])=[C:19]([CH:20]=[CH:21][CH:22]=1)[O:1][CH:2]1[CH2:3][CH2:4][CH:5]([NH:8][C:9](=[O:13])[CH:10]([CH3:11])[CH3:12])[CH2:6][CH2:7]1Participants
3
Procedure
Prepared as in Example 22b from N-(4-hydroxycyclohexyl)isobutyramide (Example 40c) and 2-amino-6-fluorobenzonitrile as an off-white solid (99%). MS 302 (MH+).
Sources & evidence
- ORD record
- ord-4e69d5a1b2c64e8ca6d0fa10a5cb0d51
- Source dataset
- uspto-grants-2013_11
- Patent number
- US08592592B2
Reaction notes
Loading…