HCID 22633460, compound → HCID 22633470, compound

HRID 398208Notes

Reaction equation

HRID 398208 reaction equation
C([O:8][C:9]1[CH:29]=[CH:28][C:12]([O:13][CH2:14][CH2:15][C:16]2[N:17]=[C:18]([C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)[O:19][C:20]=2[CH3:21])=[CH:11][C:10]=1[CH2:30][CH2:31][CH3:32])C1C=CC=CC=1.[H][H]>C(O)C.[Pd]>[CH2:30]([C:10]1[CH:11]=[C:12]([O:13][CH2:14][CH2:15][C:16]2[N:17]=[C:18]([C:22]3[CH:27]=[CH:26][C:25]([C:9]4[CH:29]=[CH:28][CH:12]=[CH:11][CH:10]=4)=[CH:24][CH:23]=3)[O:19][C:20]=2[CH3:21])[CH:28]=[CH:29][C:9]=1[OH:8])[CH2:31][CH3:32]

Participants

5

Procedure

A solution of 4-[2-(4-benzyloxy-3-propylphenoxy)ethyl]-5-methyl-2-phenyloxazole (3.16 mmol) in ethanol (100 mL) was treated with 5% Pd/C (160 mg) and hydrogen (60 psi) at ambient temperature for 18 h. The mixture was filtered and concentrated in vacuo to give a tan solid.

Workup

  1. filtrationThe mixture was filtered
  2. concentrationconcentrated in vacuo
  3. customto give a tan solid

Sources & evidence

ORD record
ord-451a9e4334064efdaa36a8d456c438ff
Source dataset
uspto-grants-2003_08
Patent number
US06610696B2

Reaction notes

Loading…