Azetidine hydrochloride → HCID 68583271, compound
Reaction equation
Cl[C:2]1[N:9]=[CH:8][C:7]([F:10])=[CH:6][C:3]=1[C:4]#[N:5].Cl.[NH:12]1[CH2:15][CH2:14][CH2:13]1>>[N:12]1([C:2]2[N:9]=[CH:8][C:7]([F:10])=[CH:6][C:3]=2[C:4]#[N:5])[CH2:15][CH2:14][CH2:13]1Participants
3
Procedure
Prepared in 78% yield from the product of Example 169A and azetidine hydrochloride according to the procedure described for Example 178A. MS (ESI+) m/z 177.8 (M+H)+; 1H NMR (DMSO-d6) δ 2.28-2.38 (m, 2H), 4.17-4.22 (m, 4H), 8.07 (dd, J=8.3, 2.9 Hz, 1H), 8.66 (dd, J=8.1, 3.0 Hz, 1H).
Sources & evidence
- ORD record
- ord-71b626f1f4184808836b7c06911b3a79
- Source dataset
- uspto-grants-2013_10
- Patent number
- US08546374B2
Reaction notes
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