Ammonia → HCID 86593026, compound
Reaction equation
C([O:8][C:9]1[CH:51]=[CH:50][C:12]([CH2:13][C@H:14]2[C@@H:18]([CH2:19][N:20]([CH2:33][CH:34]([CH3:36])[CH3:35])[S:21]([C:24]3[CH:29]=[CH:28][C:27]([N+:30]([O-])=O)=[CH:26][CH:25]=3)(=[O:23])=[O:22])[O:17][C:16]([CH3:38])([CH3:37])[N:15]2[C:39]([O:41][C@H:42]2[C@H:49]3[C@H:45]([O:46][CH2:47][CH2:48]3)[O:44][CH2:43]2)=[O:40])=[CH:11][CH:10]=1)C1C=CC=CC=1.N.[H][H]>CO.[Pd]>[NH2:30][C:27]1[CH:28]=[CH:29][C:24]([S:21]([N:20]([CH2:19][C@H:18]2[O:17][C:16]([CH3:37])([CH3:38])[N:15]([C:39]([O:41][C@H:42]3[C@H:49]4[C@H:45]([O:46][CH2:47][CH2:48]4)[O:44][CH2:43]3)=[O:40])[C@H:14]2[CH2:13][C:12]2[CH:11]=[CH:10][C:9]([OH:8])=[CH:51][CH:50]=2)[CH2:33][CH:34]([CH3:36])[CH3:35])(=[O:22])=[O:23])=[CH:25][CH:26]=1Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
To a stirred solution of (3S,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-yl (4S,5R)-4-[4-(benzyloxy)benzyl]-5-({isobutyl[(4-nitrophenyl)sulfonyl]amino}methyl)-2,2-dimethyl-1,3-oxazolidine-3-carboxylate. (0.18 g, 0.25 mmol) in 6 mL of a 2M solution of ammonia in methanol was added 0.18 g of palladium (on charcoal, 10% Pd, Degussa type). The mixture was stirred under an atmospheric pressure of hydrogen for 12 hours. The catalyst was filtered, and the solvent was removed under reduced pressure. The residue was purified on silica gel using ethyl acetate-hexanes (7:3) as eluent to provide 81 mg (54%) of the title compound.
Workup
- filtrationThe catalyst was filtered
- customthe solvent was removed under reduced pressure
- customThe residue was purified on silica gel
Sources & evidence
- ORD record
- ord-39b038ccce6e4cffac55399fe2bb9c1f
- Source dataset
- uspto-grants-2013_06
- Patent number
- US08455497B2
Reaction notes
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