HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Nitro-4-(trifluoromethyl)benzene-1-sulfonyl chloride → HCID 18511578, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Nitro-4-(trifluoromethyl)benzene-1-sulfonyl chloride | HCID 2775780 | — |
| Reactant | 3,5-Dichloro-4-(6-chloro-benzothiazol-2-yloxy)-phenylamine | HCID 22148776 | — |
| Product | HCID 18511578 | HCID 18511578 | — |
Reaction Steps
N-[3,5-Dichloro-4-(6-chloro-benzothiazol-2-yloxy)-phenyl]-2-nitro-4-trifluoromethyl-benzenesulfonamide was synthesized (48%) from 3,5-dichloro-4-(6-chloro-benzothiazol-2-yloxy)-phenylamine (420) and 2-nitro-4-trifluoromethylbenzenesulfonyl chloride (Aldrich) in a similar manner as described in Examples 70-91. 1H NMR (400 MHz, DMSO-d6) δ 11.65 (br s, 1H), 8.61 (s, 1H), 8.32-8.28 (m, 2H), 8.15 (d, J=2.2 Hz, 1H), 7.68 (d, J=8.7 Hz, 1H), 7.46 (dd, J=8.7, 2.2 Hz, 1H), 7.34 (s, 2H). MS (EI): m/z 596 (M−H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07960408B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-aa90dc8179404cc5a7760e9c36c2ce78 |
| Source note | uspto-grants-2011_06 |