4-Fluorobenzenesulfonyl chloride → HCID 68433743, compound
Reaction equation
[CH3:1][NH:2][C:3]1[C:4]2[CH:5]=[CH:6][C:7]([NH:13][CH2:14][C:15]3[O:16][C:17]([CH3:20])=[CH:18][CH:19]=3)=[N:8][C:9]=2[CH:10]=[CH:11][CH:12]=1.[F:21][C:22]1[CH:27]=[CH:26][C:25]([S:28](Cl)(=[O:30])=[O:29])=[CH:24][CH:23]=1>>[F:21][C:22]1[CH:27]=[CH:26][C:25]([S:28]([N:2]([CH3:1])[C:3]2[CH:12]=[CH:11][CH:10]=[C:9]3[C:4]=2[CH:5]=[CH:6][C:7]([NH:13][CH2:14][C:15]2[O:16][C:17]([CH3:20])=[CH:18][CH:19]=2)=[N:8]3)(=[O:30])=[O:29])=[CH:24][CH:23]=1Participants
3
Procedure
The title compound, MS: m/e=426.1 (M+H+), was prepared from N5-methyl-N2-(5-methyl-furan-2-ylmethyl)-quinoline-2,5-diamine and 4-fluorobenzene sulphonylchloride as described in example 39.
Sources & evidence
- ORD record
- ord-489a5fae72444884917b5fe0d3682391
- Source dataset
- uspto-grants-2010_11
- Patent number
- US07825253B2
Reaction notes
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