2-Amino-5-chlorobenzophenone → HCID 86683067, compound
Reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([Cl:8])=[CH:4][C:3]=1[C:9]([C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=O.[CH:17]1([C:23](=O)[CH2:24][C:25]#[N:26])[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]1>>[Cl:8][C:5]1[CH:4]=[C:3]2[C:2](=[CH:7][CH:6]=1)[N:1]=[C:23]([CH:17]1[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]1)[C:24]([C:25]#[N:26])=[C:9]2[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1Participants
3
Procedure
The title compound was prepared in analogy to example 101 step B from (2-amino-5-chlorophenyl)(phenyl)methanone and 3-cyclohexyl-3-oxo-propionitrile. Colorless solid.
Sources & evidence
- ORD record
- ord-dfeb48cd805e49dc8ee86ad3dbf0337e
- Source dataset
- uspto-grants-2015_12
- Patent number
- US09199938B2
Reaction notes
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