4-(1,3-Oxazol-5-yl)benzenesulphonyl chloride → HCID 68596862, compound
Reaction equation
[I:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][CH:6]=[CH:5]2.[O:11]1[C:15]([C:16]2[CH:21]=[CH:20][C:19]([S:22](Cl)(=[O:24])=[O:23])=[CH:18][CH:17]=2)=[CH:14][N:13]=[CH:12]1>>[I:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[N:7]([S:22]([C:19]1[CH:20]=[CH:21][C:16]([C:15]3[O:11][CH:12]=[N:13][CH:14]=3)=[CH:17][CH:18]=1)(=[O:23])=[O:24])[CH:6]=[CH:5]2Participants
3
Procedure
This compound was prepared from 5-iodo-1H-indole and 4-oxazol-5-ylbenzene-sulfonyl-chloride by the method outlined under 1.a).
Sources & evidence
- ORD record
- ord-96ea6e20b4d048abbe7dd31d74b8f92c
- Source dataset
- uspto-grants-2013_08
- Patent number
- US08507469B2
Reaction notes
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