Ammonia → HCID 10430315, compound
Reaction equation
[NH2:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][CH:6]=[C:7]2[OH:12].[OH:13][C:14]1[CH:15]=[C:16]([CH:21]=[CH:22][CH:23]=1)[C:17](OC)=O.[NH3:24]>>[NH2:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][CH:6]=[C:7]2[O:12][CH2:4][CH2:5][CH2:6][CH:7]([CH3:8])[O:13][C:14]1[CH:23]=[CH:22][CH:21]=[C:16]2[C:15]=1[N:24]=[C:2]([NH2:1])[CH:3]=[CH:17]2Participants
4
Procedure
The title compound was prepared according to the procedure described in Example 92 substituting 5-amino-1-naphthol for methyl 3-hydroxybenzoate. 1H NMR (500 MHz, DMSO-d6) δ ppm 8.36 (d, 1H), 7.56 (d, 1H), 7.48 (m, 2H), 7.39 (m, 2H), 7.27 (t, 1H), 7.17 (m, 1H), 7.12 (d, 1H), 6.87 (d, 1H), 6.80 (d, 1H), 4.92 (m, 1H), 4.17 (m, 2H), 2.04 (m, 4H), 1.45 (d, 3H); MS (DCI/NH3) m/z 388 [M+H]+.
Sources & evidence
- ORD record
- ord-a0fc0c74dcec4cbb848a2506034aabb0
- Source dataset
- uspto-grants-2006_01
- Patent number
- US06989392B2
Reaction notes
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