4-Fluorobenzenesulfonyl chloride → HCID 24987864, compound
Reaction equation
[CH3:1][C:2]1[O:6][C:5]([CH2:7][NH:8][C:9]2[CH:18]=[CH:17][C:16]3[C:15]([NH2:19])=[CH:14][CH:13]=[CH:12][C:11]=3[N:10]=2)=[CH:4][CH:3]=1.[F:20][C:21]1[CH:26]=[CH:25][C:24]([S:27](Cl)(=[O:29])=[O:28])=[CH:23][CH:22]=1>>[CH3:1][C:2]1[O:6][C:5]([CH2:7][NH:8][C:9]2[CH:18]=[CH:17][C:16]3[C:11](=[CH:12][CH:13]=[CH:14][C:15]=3[NH:19][S:27]([C:24]3[CH:25]=[CH:26][C:21]([F:20])=[CH:22][CH:23]=3)(=[O:29])=[O:28])[N:10]=2)=[CH:4][CH:3]=1Participants
3
Procedure
The title compound, MS: m/e=412.4 (M+H+), was prepared in accordance with the general method of example 39 from N2-(5-methyl-furan-2-ylmethyl)-quinoline-2,5-diamine and 4-fluorobenzenesulfonylchloride.
Sources & evidence
- ORD record
- ord-d04369702c7d4af29c778160b63891b8
- Source dataset
- uspto-grants-2010_11
- Patent number
- US07825253B2
Reaction notes
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