Ammonia → HCID 86593026, compound

HRID 1253966Notes

Reaction equation

HRID 1253966 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]=1

Participants

6

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

  1. filtrationThe catalyst was filtered
  2. customthe solvent was removed under reduced pressure
  3. 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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