4-Bromo-2-(Trifluoromethoxy)Benzene-1-Sulfonyl Chloride → 4-Bromo-N-[3,5-dichloro-4-(6-chlorobenzothiazol-2-yloxy)-phenyl]-2-trifluoromethoxy-benzenesulfonamide

Participants

Role	Name	HCID	Charge
Reactant	4-Bromo-2-(Trifluoromethoxy)Benzene-1-Sulfonyl Chloride	HCID 2736421	—
Reactant	3,5-Dichloro-4-(6-chloro-benzothiazol-2-yloxy)-phenylamine	HCID 22148776	—
Product	4-Bromo-N-[3,5-dichloro-4-(6-chlorobenzothiazol-2-yloxy)-phenyl]-2-trifluoromethoxy-benzenesulfonamide	HCID 18511570	—

Reaction Steps

4-Bromo-N-[3,5-dichloro-4-(6-chloro-benzothiazol-2-yloxy)-phenyl]-2-trifluoromethoxy-benzenesulfonamide was synthesized (83%) from 3,5-dichloro-4-(6-chloro-benzothiazol-2-yloxy)-phenylamine (420) and 4-bromo-2-trifluoromethoxybenzenesulfonyl chloride (Maybridge) in a similar manner as described in Examples 70-91.

Provenance & Evidence

DOI	10.6084/m9.figshare.5104873.v1
Patent number	US06583157B2
Source dataset	uspto-grants-2003_06
ORD ID	ord-68ba85c7c50e4c948254747da9cedeb4
Source note	uspto-grants-2003_06