Guanidine Hydrochloride → HCID 59851096, compound
Reaction equation
C([O-])(O)=O.[Na+].Cl.[NH2:7][C:8]([NH2:10])=[NH:9].[Cl:11][C:12]1[CH:13]=[CH:14][C:15]2[C:21](=O)[C:20](=[CH:23]N(C)C)[CH2:19][C:18](=[O:27])[NH:17][C:16]=2[CH:28]=1>>[NH2:9][C:8]1[N:10]=[CH:23][C:20]2[CH2:19][C:18](=[O:27])[NH:17][C:16]3[CH:28]=[C:12]([Cl:11])[CH:13]=[CH:14][C:15]=3[C:21]=2[N:7]=1Participants
4
Procedure
In a manner similar to that described for method I (NaHCO3 used instead of K2CO3), guanidine hydrochloride and 8-chloro-4-((dimethylamino)methylene)-3,4-dihydro-1H-benzo[b]azepine-2,5-dione (v-j) were converted to I-23 (72%): HRMS Calcd. for C12H9ClN4O: 261.0543, Found 261.0543.
Sources & evidence
- ORD record
- ord-1e150555ed514ef283f56ea43aba22eb
- Source dataset
- uspto-grants-2008_12
- Patent number
- US07459448B2
Reaction notes
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