HCID 54374393, compound → HCID 136016629, compound

HRID 1738369Notes

Reaction equation

HRID 1738369 reaction equation
[CH3:1][CH:2]([C:4]1[N:5]=[C:6]([C:12]2[C:17]([Cl:18])=[CH:16][CH:15]=[CH:14][C:13]=2[O:19]CC2C=CC=CC=2)[O:7][C:8]=1[O:9][CH2:10][CH3:11])[CH3:3]>C(OCC)(=O)C.[Pd]>[CH3:1][CH:2]([C:4]1[N:5]=[C:6]([C:12]2[C:13]([OH:19])=[CH:14][CH:15]=[CH:16][C:17]=2[Cl:18])[O:7][C:8]=1[O:9][CH2:10][CH3:11])[CH3:3]

Participants

4

Procedure

0.4 g 4-(2-propyl)-5-ethoxy-2-(2-benzyloxy-6-chlorophenyl)oxazole was dissolved in 10 ml ethyl acetate. To the solution, 5% palladium/carbon in an amount of 0.11 g was further added, and the solution was stirred under hydrogen atmosphere for 15-30 min. at room temperature. The solution reacted was filtrated, then the filtrate was condensed under reduced pressure, affording the objective substance in an amount of 0.28 g.

Workup

  1. customThe solution reacted
  2. filtrationwas filtrated
  3. customcondensed under reduced pressure
  4. customaffording the objective substance in an amount of 0.28 g

Sources & evidence

ORD record
ord-73de7f64eff848c9aee102d1cff4de2c
Source dataset
uspto-grants-1999_10
Patent number
US05962685

Reaction notes

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