Ethynylcyclohexane → HCID 66746496, compound
Reaction equation
[C:1]([CH:3]1[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]1)#[CH:2].[NH2:9][C:10]1[CH:17]=[CH:16][CH:15]=[C:14](Br)[C:11]=1[C:12]#[N:13]>>[NH2:9][C:10]1[CH:17]=[CH:16][CH:15]=[C:14]([C:2]#[C:1][CH:3]2[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]2)[C:11]=1[C:12]#[N:13]Participants
3
Procedure
Prepared as in Example 21c from ethynylcyclohexane and 2-amino-6-bromobenzonitrile as a brown oil (100%). 1H NMR (400 MHz, DMSO-d6) δ 1.24-1.77 (m, 10H), 2.70 (m, 1H), 6.13 (s, 2H), 6.64 (d, J=8.0 Hz, 1H), 6.74 (d, J=8.0 Hz, 1H), 7.22 (t, J=8.0 Hz, 1H). MS 225 (MH+).
Sources & evidence
- ORD record
- ord-155a3f434f9b47779fb8b1e3bcadcb9a
- Source dataset
- uspto-grants-2015_04
- Patent number
- US09000054B2
Reaction notes
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