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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1819810Generated: October 26, 2026

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

https://huagongshe.com/reaction/1819810

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-2-(Trifluoromethoxy)Benzene-1-Sulfonyl ChlorideHCID 2736421—
Reactant3,5-Dichloro-4-(6-chloro-benzothiazol-2-yloxy)-phenylamineHCID 22148776—
Product4-Bromo-N-[3,5-dichloro-4-(6-chlorobenzothiazol-2-yloxy)-phenyl]-2-trifluoromethoxy-benzenesulfonamideHCID 18511570—

Reaction Steps

4-Bromo-N-[3,5-dichloro-4-(6-chlorobenzothiazol-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. 1H NMR (400 MHz, DMSO-d6) δ 11.37 (s, 1H), 8.16 (d, J=2.2 Hz, 1H), 8.03 (d, J=8.8 Hz, 1H), 7.91-7.87 (m, 2H), 7.68 (d, J=8.7 Hz, 1H), 7.47 (d, J=8.7, 2.2 Hz, 1H), 7.31 (s, 2H). MS (EI): m/z 645 (M−H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601841B2
Source datasetuspto-grants-2009_10
ORD IDord-042de980b2c14ceab03e69e6f331838d
Source noteuspto-grants-2009_10