HCID 67069928, compound → HCID 11426956, compound
Reaction equation
C([O:8][C:9]1[CH:14]=[CH:13][C:12]([C:15]2[CH:16]=[N:17][C:18]([O:21][C@@H:22]3[CH:27]4[CH2:28][CH2:29][N:24]([CH2:25][CH2:26]4)[CH2:23]3)=[N:19][CH:20]=2)=[CH:11][C:10]=1[N+:30]([O-])=O)C1C=CC=CC=1>[Pd]>[NH2:30][C:10]1[CH:11]=[C:12]([C:15]2[CH:16]=[N:17][C:18]([O:21][C@@H:22]3[CH:27]4[CH2:26][CH2:25][N:24]([CH2:29][CH2:28]4)[CH2:23]3)=[N:19][CH:20]=2)[CH:13]=[CH:14][C:9]=1[OH:8]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
The product of Example 33C (380 mg, 0.88) was hydrogenated under the catalysis of Pd/C (Aldrich, 10 wt. %, 100 mg) according to the procedure of Example 28E. The title compound was obtained as yellow solid (220 mg, yield, 92%). 1H NMR (300 MHz, CD3OD) δ 1.47-1.93 (m, 3H), 1.95-2.35 (m, 2H) 2.70-3.05 (m, 5H), 3.33-3.48 (m, 1H), 5.04-5.30 (m, J=8.8 Hz, 1H), 6.72-6.88 (m, 2H), 6.98 (d, J=1.7 Hz, 1H), 8.70 (s, 2H) ppm. MS (DCI/NH3): 313 (M+H)+.
Sources & evidence
- ORD record
- ord-f040ac992b3445ac970fc8b315795e6e
- Source dataset
- uspto-grants-2010_02
- Patent number
- US07655657B2
Reaction notes
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