4-Nitrophenol → HCID 59987435, compound
Reaction equation
[CH3:1][NH:2][C:3]([C:5]1[CH:10]=[C:9]([CH2:11][O:12][C:13]2[CH:18]=[CH:17][C:16](N)=[CH:15][CH:14]=2)[CH:8]=[CH:7][N:6]=1)=[O:4].[N+:20](C1C=CC(O)=CC=1)([O-])=O>>[CH3:1][NH:2][C:3]([C:5]1[CH:10]=[C:9]([CH2:11][O:12][C:13]2[CH:18]=[CH:17][CH:16]=[C:15]([NH2:20])[CH:14]=2)[CH:8]=[CH:7][N:6]=1)=[O:4]Participants
3
Procedure
The title compound was prepared in the same manner described for 4-(4-aminophenoxymethyl)pyridine-2-carboxylic acid methylamide, substituting 3-nitrophenol for 4-nitrophenol. 1H-NMR (CD3OD) δ 8.40 (d, J=4.5 Hz, 1H), 7.54 (d, J=2.1 Hz, 1H), 7.13 (t, J=6.3 Hz, 1H), 7.00 (dd, J=4.2, 1.8 Hz, 1H), 6.62 to 6.59 (m, 1H), 6.43 (t, J=1.8 Hz, 1H), 6.37 to 6.34 (m, 1H), 4.89 (s, 2H), 2.93 (s, 3H).
Sources & evidence
- ORD record
- ord-e7f1af966cba4a30a4b009bd97b3531c
- Source dataset
- uspto-grants-2011_12
- Patent number
- US08076488B2
Reaction notes
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