Hydrochloric Acid → HCID 12083250, compound

HRID 398194Notes

Reaction equation

HRID 398194 reaction equation
C([O:3][C:4](=[O:36])[C:5]([CH3:35])([O:7][C:8]1[CH:13]=[CH:12][C:11]([S:14][CH2:15][CH2:16][C:17]2[N:18]=[C:19]([C:23]3[CH:28]=[CH:27][C:26]([C:29]4[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=4)=[CH:25][CH:24]=3)[O:20][C:21]=2[CH3:22])=[CH:10][CH:9]=1)[CH3:6])C.[OH-].[Na+].Cl>CCO>[C:26]1([C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)[CH:25]=[CH:24][C:23]([C:19]2[O:20][C:21]([CH3:22])=[C:17]([CH2:16][CH2:15][S:14][C:11]3[CH:12]=[CH:13][C:8]([O:7][C:5]([CH3:35])([CH3:6])[C:4]([OH:36])=[O:3])=[CH:9][CH:10]=3)[N:18]=2)=[CH:28][CH:27]=1

Participants

5

Procedure

2-Methyl-2-{4-[2-(5-methyl-2-biphenyl-4-yl-oxazol-4-yl)ethylsulfanyl]phenoxy}propionic acid ethyl ester (0.23 mmol) was dissolved in EtOH (10 mL) and 5N NaOH (0.5 mL) was added. The reaction was stirred overnight at room temperature. The reaction was acidified with 5N HCl and the product was extracted into ethyl acetate, dried (MgSO4) and concentrated to give 96 mg crude product.

Workup

  1. extractionthe product was extracted into ethyl acetate
  2. dry with materialdried (MgSO4)
  3. concentrationconcentrated

Sources & evidence

ORD record
ord-8d786462a34b43988ac570122a4503c9
Source dataset
uspto-grants-2003_08
Patent number
US06610696B2

Reaction notes

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