Reaction equation
[Cl:1][C:2]1[CH2:6][CH2:5][CH2:4][N:3]=1.[CH3:7][C:8]1[C:14]([N+:15]([O-])=O)=[CH:13][CH:12]=[CH:11][C:9]=1[NH2:10]>>[ClH:1].[ClH:1].[CH3:7][C:8]1[C:9]([NH2:10])=[CH:11][CH:12]=[CH:13][C:14]=1[NH:15][C:2]1[CH2:6][CH2:5][CH2:4][N:3]=1Participants
3
Procedure
The title compound (20.9 g) was prepared by the methods of Examples 8 and 9 using 2-chloro-1-pyrroline, prepared as in Example 1, and 30.0 g of 2-methyl-3-nitroaniline. Structure assignment was supported by the nmr spectrum and by elemental analysis.
Sources & evidence
- ORD record
- ord-295562804b2b4a26953fd879ae21187d
- Source dataset
- uspto-grants-1985_08
- Patent number
- US04533739
Linked notes
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