Hydrochloric Acid → [2'-(1-Ethyl-3-methyl-ureidomethyl)-5,4'-bis-trifluoromethyl-biphenyl-3-yl]-acetic acid

HRID 563554Notes

Reaction equation

HRID 563554 reaction equation
C[O:2][C:3](=[O:33])[CH2:4][C:5]1[CH:6]=[C:7]([C:15]2[CH:20]=[CH:19][C:18]([C:21]([F:24])([F:23])[F:22])=[CH:17][C:16]=2[CH2:25][N:26]([CH2:31][CH3:32])[C:27]([NH:29][CH3:30])=[O:28])[CH:8]=[C:9]([C:11]([F:14])([F:13])[F:12])[CH:10]=1.[Li+].[OH-].Cl>O1CCOCC1>[CH2:31]([N:26]([CH2:25][C:16]1[CH:17]=[C:18]([C:21]([F:23])([F:24])[F:22])[CH:19]=[CH:20][C:15]=1[C:7]1[CH:8]=[C:9]([C:11]([F:12])([F:13])[F:14])[CH:10]=[C:5]([CH2:4][C:3]([OH:33])=[O:2])[CH:6]=1)[C:27]([NH:29][CH3:30])=[O:28])[CH3:32]

Participants

5

Procedure

To [2′-(1-ethyl-3-methyl-ureidomethyl)-5,4′-bis-trifluoromethyl-biphenyl-3-yl]-acetic acid methyl ester (0.18 mmol) was added 1:1 1N aqueous LiOH: 1,4-dioxane (2 mL), and the reaction was stirred at room temperature for 30 minutes. 10% Aqueous HCl was added to acidify the solution to pH 3, and the mixture was extracted with EtOAc. The crude material was purified by silica gel chromatography to give the title compound. M+H is 463.

Workup

  1. extractionthe mixture was extracted with EtOAc
  2. customThe crude material was purified by silica gel chromatography

Sources & evidence

ORD record
ord-2ff5ab93d8554692b749b4539ffdc43f
Source dataset
uspto-grants-2011_11
Patent number
US08067445B2

Reaction notes

Loading…