Isobutyryl chloride → HCID 44159062, compound
Reaction equation
C([O:3][C:4](=[O:28])[CH2:5][C:6]1[CH:7]=[C:8]([C:14]2[CH:19]=[CH:18][C:17]([C:20]([F:23])([F:22])[F:21])=[CH:16][C:15]=2[CH2:24][NH:25][CH2:26][CH3:27])[C:9]([O:12][CH3:13])=[CH:10][CH:11]=1)C.[C:29](Cl)(=[O:33])[CH:30]([CH3:32])[CH3:31]>>[CH2:26]([N:25]([CH2:24][C:15]1[CH:16]=[C:17]([C:20]([F:21])([F:22])[F:23])[CH:18]=[CH:19][C:14]=1[C:8]1[C:9]([O:12][CH3:13])=[CH:10][CH:11]=[C:6]([CH2:5][C:4]([OH:3])=[O:28])[CH:7]=1)[C:29](=[O:33])[CH:30]([CH3:32])[CH3:31])[CH3:27]Participants
3
Procedure
{2′-[(Ethyl-isobutyryl-amino)-methyl]-6-methoxy-4′-trifluoromethyl-biphenyl-3-yl}-acetic acid (Compound 1-246) was prepared using the procedures of Example 1 and using (2′-ethylaminomethyl-6-methoxy-4′-trifluoromethyl-biphenyl-3-yl)-acetic acid ethyl ester and isobutyryl chloride.
Sources & evidence
- ORD record
- ord-a1d4822faaab4649826d673e9e8ad60d
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08168678B2
Reaction notes
Loading…