HCID 21458444, compound → HCID 21458453, compound
Reaction equation
C([N:8]1[CH2:19][CH2:18][N:17](CC2C=CC=CC=2)[CH2:16][CH2:15][N:14](CC2C=CC=CC=2)[CH2:13][CH2:12][N:11]([CH2:34][C:35](=[O:82])[NH:36][CH2:37][CH2:38][O:39][CH2:40][CH2:41][O:42][CH2:43][CH2:44][NH:45][C:46](=[O:81])[CH2:47][N:48]2[CH2:59][CH2:58][N:57](CC3C=CC=CC=3)[CH2:56][CH2:55][N:54](CC3C=CC=CC=3)[CH2:53][CH2:52][N:51](CC3C=CC=CC=3)[CH2:50][CH2:49]2)[CH2:10][CH2:9]1)C1C=CC=CC=1.[H][H]>[Pd].C(O)C>[N:11]1([CH2:34][C:35](=[O:82])[NH:36][CH2:37][CH2:38][O:39][CH2:40][CH2:41][O:42][CH2:43][CH2:44][NH:45][C:46](=[O:81])[CH2:47][N:48]2[CH2:59][CH2:58][NH:57][CH2:56][CH2:55][NH:54][CH2:53][CH2:52][NH:51][CH2:50][CH2:49]2)[CH2:12][CH2:13][NH:14][CH2:15][CH2:16][NH:17][CH2:18][CH2:19][NH:8][CH2:9][CH2:10]1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
A 100 mL Autoclave pressure reactor was charged with 9.2 g (8.3 mmol) of 8, 50 mL of ethanol and 3 g of 10% Pd/C. The reactor was pressurized to 220 psig with hydrogen for 3 hours at 80° C. The mixture was filtered and the filtrate was concentrated to a slightly yellow oil. 1H NMR, 13C NMR, and mass spectroscopy data were consistent with 9. The yield of 9 was essentially quantitative.
Workup
- filtrationThe mixture was filtered
- concentrationthe filtrate was concentrated to a slightly yellow oil
Sources & evidence
- ORD record
- ord-f5175069896246cbab542c66fdb8935d
- Source dataset
- uspto-grants-1998_01
- Patent number
- US05705637
Reaction notes
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