HuagongsheHuagongshe Chemistry Print Report · For research reference only
9-Aminoacridine → HCID 54507950, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 9-Aminoacridine | HCID 7019 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Mesitylenesulfonyl chloride | HCID 13046 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 54507950 | HCID 54507950 | 6% |
Reaction Steps
To a suspension of 4.00 g (20.6 mmol) of 9-aminoacridine 40 in 350 mL of CHCl3 was added 2.9 mL (20.8 mmol) of Et3N and 4.50 g (20.6 mmol) of mesitylenesulfonyl chloride. The reaction mixture was refluxed for 72 hr. Then the reaction mixture was filtered and the solvent was evaporated. The material was purified by column chromatography on silica gel by eluting first with 1% MeOH in CH2Cl2 and then with 5% MeOH in CH2Cl2 to yield 458.4 mg (6%) of sulfonamide 41 as an orange solid: 1H NMR (300 MHz, CDCl3, TMS) δ 9.25 (s, 1H), 8.77 (d, J=8 Hz, 2H), 7.46 (t, J=8 Hz, 2H), 7.21 (d, J=8 Hz, 2H), 7.15 (t, J=8 Hz, 2H), 7.02 (s, 2H), 2.78 (s, 6H), 2.36 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07253207B2 |
| Source dataset | uspto-grants-2007_08 |
| ORD ID | ord-336a936b38114919bac188c2e64f3194 |
| Source note | uspto-grants-2007_08 |