Butyryl chloride → 2-[(2-Methyl-4-(butanamido)phenyl)amino]-1-pyrroline, hydrochloride
Reaction equation
[C:1]([Cl:6])(=[O:5])[CH2:2][CH2:3][CH3:4].Cl.Cl.[CH3:9][C:10]1[CH:15]=[C:14]([NH2:16])[CH:13]=[CH:12][C:11]=1[NH:17][C:18]1[CH2:22][CH2:21][CH2:20][N:19]=1>>[ClH:6].[CH3:9][C:10]1[CH:15]=[C:14]([NH:16][C:1](=[O:5])[CH2:2][CH2:3][CH3:4])[CH:13]=[CH:12][C:11]=1[NH:17][C:18]1[CH2:22][CH2:21][CH2:20][N:19]=1Participants
3
Procedure
The title compound was prepared by the method of Example 21 using 30.5 mmole of butanoyl chloride and 1.0 g (3.8 mmole) of the product compound of Example 9. Structure assignment was supported by the nmr spectrum and by elemental analysis.
Sources & evidence
- ORD record
- ord-3fcef290bd9e44f3ad84d376408c30b1
- Source dataset
- uspto-grants-1985_08
- Patent number
- US04533739
Reaction notes
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