Ethyl formate → HCID 178522218, compound
Reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8]/[C:9](=[C:16]2\[C:17](=[O:28])[NH:18][C:19]3[C:24]\2=[CH:23][C:22]([N+:25]([O-:27])=[O:26])=[CH:21][CH:20]=3)/[C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[CH:4][CH:3]=1.[CH:29](OCC)=[O:30]>CN(C=O)C>[CH:29]([NH:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8]/[C:9](=[C:16]2\[C:17](=[O:28])[NH:18][C:19]3[C:24]\2=[CH:23][C:22]([N+:25]([O-:27])=[O:26])=[CH:21][CH:20]=3)/[C:10]2[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=2)=[CH:4][CH:3]=1)=[O:30]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Prepared analogously to Example 29b from (Z)-3-[1-(4-aminophenylamino)-1-phenyl-methylidene}-5-nitro-2-indolinone and ethyl formate in DMF.
Sources & evidence
- ORD record
- ord-de9f0099a7e84ea4881a0c6c989ed158
- Source dataset
- uspto-grants-2005_02
- Patent number
- US06855710B2
Reaction notes
Loading…