HuagongsheHuagongshe Chemistry Print Report · For research reference only
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-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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07601841B2 |
| Source dataset | uspto-grants-2009_10 |
| ORD ID | ord-042de980b2c14ceab03e69e6f331838d |
| Source note | uspto-grants-2009_10 |