1-(2-(4-(6-FLUORO-1,2-BENZISOXAZOL-3-YL)-1-PIPERIDINYL)ETHYL)-3-PHENYL-2-IMIDAZOLIDINONE → HCID 18663208, compound
Reaction equation
[F:1][C:2]1[CH:30]=[CH:29][C:5]2[C:6]([CH:9]3[CH2:14][CH2:13][N:12]([CH2:15][CH2:16][N:17]4[CH2:21][CH2:20][N:19]([C:22]5[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=5)[C:18]4=[O:28])[CH2:11][CH2:10]3)=[N:7][O:8][C:4]=2[CH:3]=1.[OH:31]C1C=CC(N=C=O)=CC=1>>[F:1][C:2]1[CH:30]=[CH:29][C:5]2[C:6]([CH:9]3[CH2:14][CH2:13][N:12]([CH2:15][CH2:16][N:17]4[CH2:21][CH2:20][N:19]([C:22]5[CH:27]=[CH:26][C:25]([OH:31])=[CH:24][CH:23]=5)[C:18]4=[O:28])[CH2:11][CH2:10]3)=[N:7][O:8][C:4]=2[CH:3]=1Participants
3
Procedure
This product is obtained in the same manner as the compound of Example 5, but with replacement of the phenyl isocyanate by 4-hydroxyphenyl isocyanate in Step 1 of the synthesis. The expected product melts at 190°-194° C.
Sources & evidence
- ORD record
- ord-0c9ddfeecddd496fb0ee1542a8e551ee
- Source dataset
- uspto-grants-1998_07