Iodine → HCID 68479364, compound
Reaction equation
[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[N:7]([CH2:11][C:12]([OH:14])=[O:13])[C:6]([CH3:15])=[CH:5]2.II.[F:18][C:19]([F:28])([F:27])[C:20]1[CH:25]=[CH:24][C:23]([SH:26])=[CH:22][CH:21]=1>>[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[N:7]([CH2:11][C:12]([OH:14])=[O:13])[C:6]([CH3:15])=[C:5]2[S:26][C:23]1[CH:22]=[CH:21][C:20]([C:19]([F:18])([F:27])[F:28])=[CH:25][CH:24]=1Participants
4
Procedure
Prepared by the method of example 26 step c) using the product of example 26 step b) (0.55 g), iodine (0.98 g) and 4-trifluoromethylbenzenethiol (0.67 g) to give the subtitle compound as a solid (0.25 g).
Workup
- customPrepared by the method of example 26 step c)
Sources & evidence
- ORD record
- ord-a51a91ddc88a4d7db2afe39ac0ce1525
- Source dataset
- uspto-grants-2010_05
- Patent number
- US07723373B2
Reaction notes
Loading…