2-Amino-6-bromobenzonitrile → HCID 67400820, compound
Reaction equation
[CH3:1][O:2][CH2:3][C@@H:4]1[CH2:6][C@H:5]1B(O)O.[NH2:10][C:11]1[CH:18]=[CH:17][CH:16]=[C:15](Br)[C:12]=1[C:13]#[N:14]>>[NH2:10][C:11]1[CH:18]=[CH:17][CH:16]=[C:15]([C@@H:5]2[CH2:6][C@H:4]2[CH2:3][O:2][CH3:1])[C:12]=1[C:13]#[N:14]Participants
3
Procedure
Prepared as in Example 270a from (±)-trans-2-(methoxymethyl)cyclopropylboronic acid (example 271b) and 2-amino-6-bromobenzonitrile in 64% yield as a yellowish brown waxy solid. 1H NMR (400 MHz, DMSO-d6) δ 0.932 (m, 2H), 1.341 (m, 1H), 1.879 (m, 1H), 2.324 (s, 3H), 3.351 (d, J=6 Hz, 2H), 5.896 (br. s, 2H), 6.148 (d, J=8 Hz, 1H), 6.550 (d, J=8 Hz, 1H), 7.130 (t, J=8 Hz, 1H).
Sources & evidence
- ORD record
- ord-abc608da42e645fca79b155136c54d2e
- Source dataset
- uspto-grants-2015_11
- Patent number
- US09181276B2
Reaction notes
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