4-Fluoro-3-(trifluoromethyl)benzenesulfonyl Chloride → N-[6-(4-Chloro-benzyloxymethyl)-pyridin-2-yl]-4-fluoro-3-trifluoromethyl-benzenesulfonamide

HRID 1454907

Reaction equation

HRID 1454907 reaction equation
[Cl:1][C:2]1[CH:17]=[CH:16][C:5]([CH2:6][O:7][CH2:8][C:9]2[N:14]=[C:13]([NH2:15])[CH:12]=[CH:11][CH:10]=2)=[CH:4][CH:3]=1.[F:18][C:19]1[CH:24]=[CH:23][C:22]([S:25](Cl)(=[O:27])=[O:26])=[CH:21][C:20]=1[C:29]([F:32])([F:31])[F:30]>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:6][O:7][CH2:8][C:9]2[N:14]=[C:13]([NH:15][S:25]([C:22]3[CH:23]=[CH:24][C:19]([F:18])=[C:20]([C:29]([F:32])([F:30])[F:31])[CH:21]=3)(=[O:27])=[O:26])[CH:12]=[CH:11][CH:10]=2)=[CH:16][CH:17]=1

Participants

3

Reactant 2

HCID 27375494-Fluoro-3-(trifluoromethyl)benzenesulfonyl ChlorideHCID 688451046-(4-Chloro-benzyloxymethyl)-pyridin-2-ylamine

Product 1

HCID 68845596N-[6-(4-Chloro-benzyloxymethyl)-pyridin-2-yl]-4-fluoro-3-trifluoromethyl-benzenesulfonamide

Procedure

This material was prepared in analogy to example 1 from 6-(4-chloro-benzyloxymethyl)-pyridin-2-ylamine (0.08 g) and 4-fluoro-3-(trifluoromethyl)-benzenesulfonyl chloride (0.092g) as a light yellow gum (0.039 g). MS (ESI−): 472.8 ([M−H]−).

Sources & evidence

ORD record
ord-7174d804faf74439bd5d185ef6bb256f
Source dataset
uspto-grants-2009_01
Patent number
US07482341B2

Linked notes

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