4-(2-Chloropyridin-4-yl)-5-(4-fluorophenyl)-1,3-dihydroimidazole-2-thione → 4-(4-Fluorophenyl)-5-(2-fluoropyridin-4-yl)-1,3-dihydroimidazole-2-thione
Reaction equation
Cl.[NH2:2][CH:3]([C:13]1[CH:18]=[CH:17][N:16]=[C:15]([F:19])[CH:14]=1)[C:4]([C:6]1[CH:11]=[CH:10][C:9]([F:12])=[CH:8][CH:7]=1)=O.ClC1C=C(C2[NH:28][C:29](=[S:39])NC=2C2C=CC(F)=CC=2)C=CN=1>>[F:12][C:9]1[CH:10]=[CH:11][C:6]([C:4]2[NH:28][C:29](=[S:39])[NH:2][C:3]=2[C:13]2[CH:18]=[CH:17][N:16]=[C:15]([F:19])[CH:14]=2)=[CH:7][CH:8]=1Participants
3
Procedure
24b was prepared from 23b (6.1 g; 20 mmol) using the method described in the synthesis of 24a.
Sources & evidence
- ORD record
- ord-bc4d831c99b1445c8a11fddb9d9511de
- Source dataset
- uspto-grants-2009_09
- Patent number
- US07582660B2
Reaction notes
Loading…