Ethylamine → 3'-Ethylamino-4'-nitroacetanilide
Reaction equation
F[C:2]1[CH:3]=[C:4]([CH:9]=[CH:10][C:11]=1[N+:12]([O-:14])=[O:13])[NH:5][C:6](=[O:8])[CH3:7].[CH2:15]([NH2:17])[CH3:16]>>[CH2:15]([NH:17][C:2]1[CH:3]=[C:4]([CH:9]=[CH:10][C:11]=1[N+:12]([O-:14])=[O:13])[NH:5][C:6](=[O:8])[CH3:7])[CH3:16]Participants
3
Procedure
In a manner similar to Example 31, the title compound was prepared from 3′-fluoro-4′-nitroacetanilide and ethylamine. 1H-NMR (CDCl3): δ 8.17 (1H, brs), 8.13 (1H, d), 7.57 (1H, br d), 7.33 (1H, brs), 6.38 (1H, dd), 3.36 (2H, m), 2.22 (3H, s), 1.37 (3H, t).
Sources & evidence
- ORD record
- ord-1db8062a371f4377bfe396ac57140df1
- Source dataset
- uspto-grants-2006_10
- Patent number
- US07115640B2
Reaction notes
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