4-Fluoroaniline → 1-[(4-Fluorophenyl)carbamoyl]cyclopropanecarboxylic Acid
Reaction equation
[C:1]1([NH:7][C:8]([C:10]2([C:13]([OH:15])=[O:14])[CH2:12][CH2:11]2)=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[F:16]C1C=CC(N)=CC=1>>[F:16][C:4]1[CH:3]=[CH:2][C:1]([NH:7][C:8]([C:10]2([C:13]([OH:15])=[O:14])[CH2:11][CH2:12]2)=[O:9])=[CH:6][CH:5]=1Participants
3
Procedure
Following the procedure described above for the compound 161 (scheme 45), but replacing aniline for 4-fluoroaniline, title compound 181 was obtained in 57% yield. MS (m/z): 224.0 (M+H).
Sources & evidence
- ORD record
- ord-10603b30188d4307aa5141635e72ac86
- Source dataset
- uspto-grants-2012_12
- Patent number
- US08329726B2
Reaction notes
Loading…