HCID 56628646, compound → HCID 18703940, compound

HRID 2288101Notes

Reaction equation

HRID 2288101 reaction equation
C1(C([O:14][C:15]([C:17]23[C:28]4([CH:30]=[O:31])[CH2:29][CH:20]([C:21]2([CH2:33][O:34][C:35]25[CH:48]([OH:49])[CH:41]6[CH:42]([O:43][CH2:44][C:45]([NH2:47])=[O:46])[CH:37]([CH:38]([O:40]6)[O:39]2)[O:36]5)[CH2:22][CH:23]2[CH:27]4[CH2:26][CH2:25][CH:24]2[CH3:32])[CH:19]=[C:18]3[CH:50]([CH3:52])[CH3:51])=[O:16])C2C=CC=CC=2)C=CC=CC=1>C(OCC)(=O)C.[C].[Pd]>[NH2:47][C:45]([CH2:44][O:43][CH:42]1[CH:37]2[CH:38]3[O:39][C:35]([O:34][CH2:33][C:21]45[CH:20]6[CH2:29][C:28]([CH:30]=[O:31])([C:17]4([C:15]([OH:16])=[O:14])[C:18]([CH:50]([CH3:51])[CH3:52])=[CH:19]6)[CH:27]4[CH:23]([CH:24]([CH3:32])[CH2:25][CH2:26]4)[CH2:22]5)([CH:48]([OH:49])[CH:41]1[O:40]3)[O:36]2)=[O:46]

Participants

4

Procedure

14 mg of compound (70) was dissolved in 3 ml of ethyl acetate and stirred together with a catalytic amount of 10% palladium-carbon under a hydrogen atmosphere at room temperature for 1.5 hours. The reaction solution was filtered and concentrated in vacuo. The reaction product was dissolved in 10 ml of methanol and washed with 10 ml of n-hexane four times, and the lower layer was concentrated in vacuo to give 8.6 mg of compound (71) as a colorless solid.

Workup

  1. filtrationThe reaction solution was filtered
  2. concentrationconcentrated in vacuo
  3. dissolutionThe reaction product was dissolved in 10 ml of methanol
  4. washwashed with 10 ml of n-hexane four times
  5. concentrationthe lower layer was concentrated in vacuo

Sources & evidence

ORD record
ord-42a9a729e7a3460cbd1596d9b7d3121e
Source dataset
uspto-grants-2000_07
Patent number
US06087390

Reaction notes

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