3-Fluoro-4-methylbenzene-1-sulfonyl chloride → N-(5-Chloro-6-(quinolin-3-yloxy)pyridin-3-yl)-3-fluoro-4-methylbenzenesulfonamide

HRID 2388081Notes

Reaction equation

HRID 2388081 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([NH2:19])[CH:5]=[N:6][C:7]=1[O:8][C:9]1[CH:10]=[N:11][C:12]2[C:17]([CH:18]=1)=[CH:16][CH:15]=[CH:14][CH:13]=2.[F:20][C:21]1[CH:22]=[C:23]([S:28](Cl)(=[O:30])=[O:29])[CH:24]=[CH:25][C:26]=1[CH3:27]>>[Cl:1][C:2]1[CH:3]=[C:4]([NH:19][S:28]([C:23]2[CH:24]=[CH:25][C:26]([CH3:27])=[C:21]([F:20])[CH:22]=2)(=[O:29])=[O:30])[CH:5]=[N:6][C:7]=1[O:8][C:9]1[CH:10]=[N:11][C:12]2[C:17]([CH:18]=1)=[CH:16][CH:15]=[CH:14][CH:13]=2

Participants

3

Reactant 2

HCID 27786003-Fluoro-4-methylbenzene-1-sulfonyl chlorideHCID 687907985-Chloro-6-(quinolin-3-yloxy)pyridin-3-amine

Product 1

HCID 24852916N-(5-Chloro-6-(quinolin-3-yloxy)pyridin-3-yl)-3-fluoro-4-methylbenzenesulfonamide

Procedure

The title compound was prepared by reacting 5-chloro-6-(quinolin-3-yloxy)pyridin-3-amine (obtained as per procedure described in preparation 1) and 3-fluoro-4-methylbenzene-1-sulfonyl chloride.

Sources & evidence

ORD record
ord-96c219730a59487785405e7824620396
Source dataset
uspto-grants-2012_09
Patent number
US08269010B2

Reaction notes

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