Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Nitrate | HCID 24434 | — |
| Reactant | HCID 86620264 | HCID 86620264 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | HCID 86620263 | HCID 86620263 | 21% |
Reaction Steps
Ice cold H2SO4 (98%, 5 mL) was added to 218 (30 mg, 0.069 mmol) at 0° C. with stirring. An ice-cold solution of KNO3 (9 mg, 0.089 mmol) in H2SO4 (98%, 1 mL) was then added dropwise. After 1 h the mixture was poured into ice water and extracted with EtOAc (×3). The combined EtOAc extracts were washed with H2O, brine and dried. Chromatography eluting with petroleum ether/EtOAc (1:1) gave 1-(chloromethyl)-5,7-dinitro-3-(trifluoroacetyl)-1,2-dihydro-3H-benzo[e]indole-8-sulfonamide (219) (7 mg, 21%) as an orange powder: mp 201-204° C.; 1H NMR (CDCl3) δ 9.49 (s, 1H), 9.29 (s, 1H), 8.71 (s, 1H), 5.67 (s, 2H), 4.73 (d, J=10.8 Hz, 1H), 4.62 (dd, J=11.3, 8.8 Hz, 1H), 4.52-4.45 (m, 1H), 3.97 (dd, J=11.8, 3.5 Hz, 1H), 3.85 (dd, J=11.8, 6.3 Hz, 1H). HRMS (FAB) calcd. for C15H1135ClF3N4O7S (MH+) m/z 482.9989, found 482.9988.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07718688B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-80892b7ee8a244d588a90bf1aaff1f79 |
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| Source note | uspto-grants-2010_05 |
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