Sulfuric Acid → HCID 86651107, compound
Reaction equation
C(NC(=O)[N:10]([CH2:13][C:14]1[CH:19]=[C:18]([C:20]([F:23])([F:22])[F:21])[CH:17]=[CH:16][C:15]=1[C:24]1[CH:29]=[C:28]([C:30]([F:33])([F:32])[F:31])[CH:27]=[C:26]([C@@H:34]([CH3:47])[C:35](N[C@H](C)CC2C=CC=CC=2)=[O:36])[CH:25]=1)[CH2:11][CH3:12])C1C=CC=CC=1.[OH:49]S(O)(=O)=O>O1CCOCC1>[CH2:11]([NH:10][CH2:13][C:14]1[CH:19]=[C:18]([C:20]([F:22])([F:23])[F:21])[CH:17]=[CH:16][C:15]=1[C:24]1[CH:29]=[C:28]([C:30]([F:32])([F:33])[F:31])[CH:27]=[C:26]([C@@H:34]([CH3:47])[C:35]([OH:36])=[O:49])[CH:25]=1)[CH3:12]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
(R)-2-[2′-(3-Benzyl-1-ethyl-ureidomethyl)-5,4′-bis-trifluoromethyl-biphenyl-3-yl]-N—((R)-1-methyl-2-phenyl-ethyl)-propionamide (0.08 g, 0.12 mmol) was treated with 5N aqueous H2SO4 in 1,4-dioxane at 100° C. for 24 hours. The mixture was purified by preparative HPLC to give the title compound.
Workup
- customThe mixture was purified by preparative HPLC
Sources & evidence
- ORD record
- ord-fc55e88b1f094b30a3fd9772912d1e5e
- Source dataset
- uspto-grants-2013_01
- Patent number
- US08362044B2
Reaction notes
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