HCID 86654076, compound → HCID 178509452, compound
Reaction equation
[NH:1]1[C:5]2[CH:6]=[CH:7][C:8]([C:10]([OH:12])=O)=[CH:9][C:4]=2[N:3]=[CH:2]1.[CH2:13]1[C@H:22]2[C@H:17]([CH2:18][CH2:19][C:20]3[CH:26]=[CH:25][C:24]([C:27]#[N:28])=[CH:23][C:21]=32)[NH:16][CH2:15][CH2:14]1>>[NH:1]1[C:5]2[CH:6]=[CH:7][C:8]([C:10]([N:16]3[C@@H:17]4[C@@H:22]([C:21]5[CH:23]=[C:24]([C:27]#[N:28])[CH:25]=[CH:26][C:20]=5[CH2:19][CH2:18]4)[CH2:13][CH2:14][CH2:15]3)=[O:12])=[CH:9][C:4]=2[N:3]=[CH:2]1Participants
3
Procedure
The title compound is prepared from 1H-benzoimidazole-5-carboxylic acid and cis-1,2,3,4,4a,5,6,10b-octahydro-benzo[f]quinoline-9-carbonitrile following a procedure analogous to that described in Example 1. Yield: 64% of theory; LC (method 1): tR=2.40 min; Mass spectrum (ESI+): m/z=357 [M+H]+.
Sources & evidence
- ORD record
- ord-d145920a5a2f41c9824d57298caf8007
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09120769B2
Reaction notes
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