HCID 67217405, compound → HCID 23627457, compound
Reaction equation
[C:1]1([CH3:28])[CH:6]=[CH:5][C:4]([S:7]([N:10]2[CH:23]([CH2:24][C:25](O)=[O:26])[C:22]3[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=3)[C:16]3[CH:15]=[CH:14][CH:13]=[CH:12][C:11]2=3)(=[O:9])=[O:8])=[CH:3][CH:2]=1.[ClH:29].Cl.[NH:31]1[CH2:35][CH2:34][N:33]=[C:32]1[C:36]1[CH:41]=[CH:40][C:39]([CH2:42][CH2:43][NH2:44])=[CH:38][CH:37]=1>>[ClH:29].[NH:33]1[CH2:34][CH2:35][N:31]=[C:32]1[C:36]1[CH:37]=[CH:38][C:39]([CH2:42][CH2:43][NH:44][C:25](=[O:26])[CH2:24][CH:23]2[C:22]3[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=3)[C:16]3[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=3[N:10]2[S:7]([C:4]2[CH:3]=[CH:2][C:1]([CH3:28])=[CH:6][CH:5]=2)(=[O:9])=[O:8])=[CH:40][CH:41]=1Participants
3
Procedure
The title compound was prepared from [5-(toluene-4-sulfonyl)-5,6-dihydro-phenanthridin-6-yl]-acetic acid and 2-[4-(4,5-dihydro-1H-imidazol-2-yl)-phenyl]-ethylamine dihydrochloride (Reference Example 2) according to the method described in Example 1e. MS (EI) 565.7 (MH+).
Sources & evidence
- ORD record
- ord-0a0b476b504e4316a137ad0a11a97fb3
- Source dataset
- uspto-grants-2011_10
- Patent number
- US08034827B2
Reaction notes
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