2-Mesitylenesulfonyl chloride → HCID 24852918, compound

HRID 2388083Notes

Reaction equation

HRID 2388083 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.[CH3:20][C:21]1[CH:26]=[C:25]([CH3:27])[CH:24]=[C:23]([CH3:28])[C:22]=1[S:29](Cl)(=[O:31])=[O:30]>>[Cl:1][C:2]1[CH:3]=[C:4]([NH:19][S:29]([C:22]2[C:23]([CH3:28])=[CH:24][C:25]([CH3:27])=[CH:26][C:21]=2[CH3:20])(=[O:31])=[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 130462-Mesitylenesulfonyl chlorideHCID 687907985-Chloro-6-(quinolin-3-yloxy)pyridin-3-amine

Product 1

HCID 24852918HCID 24852918, compound

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 2,4,6-trimethylbenzene-1-sulfonyl chloride.

Sources & evidence

ORD record
ord-c407416382474d1cb6ce307e41f58cbd
Source dataset
uspto-grants-2012_09
Patent number
US08269010B2

Reaction notes

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