4-(4-Chlorophenyl)dihydro-2H-pyran-2,6(3H)-dione → HCID 45380883, compound
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([NH2:8])=[C:4]([NH2:9])[CH:3]=1.[Cl:10][C:11]1[CH:16]=[CH:15][C:14]([CH:17]2[CH2:23][C:22](=O)[O:21][C:19](=[O:20])[CH2:18]2)=[CH:13][CH:12]=1>>[Cl:10][C:11]1[CH:12]=[CH:13][C:14]([CH:17]([CH2:23][C:22]2[NH:9][C:4]3[CH:3]=[C:2]([F:1])[CH:7]=[CH:6][C:5]=3[N:8]=2)[CH2:18][C:19]([OH:21])=[O:20])=[CH:15][CH:16]=1.[ClH:10]Participants
3
Procedure
By a procedure similar to that of 1.4, starting from commercial 4-fluoro-1,2-phenylenediamine and 3-(4-chlorophenyl)glutaric anhydride, 3-(4-chlorophenyl)-4-(5-fluoro-2-benzimidazolyl)butanoic acid•HCl was obtained as colourless solid.
Sources & evidence
- ORD record
- ord-97daf22cb2b747c7bc72af55518e030b
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08912186B2
Reaction notes
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