Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | HCID 25140917 | HCID 25140917 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 135899475 | HCID 135899475 | 53.4% |
Reaction Steps
H2O2 (70%, 0.18 mL, ca. 3.6 mmol) was added dropwise to a stirred solution of TFAA (0.51 mL, 3.6 mmol) in DCM (6 mL) at 0° C. The solution was stirred at 20° C. for 10 min, then cooled to 0° C., added to a solution of 1-oxide 207 (100 mg, 0.36 mmol) and TFA (0.06 mL, 0.78 mmol) in CHCl3 (6 mL) at 0° C. and the solution stirred at 20° C. for 4.5 h. The solution was cooled to 0° C., made basic with dilute aqueous NH3 solution and extracted with CHCl3 (3×10 mL). The combined organic fraction was dried and the solvent evaporated. The residue was purified by chromatography, eluting with a gradient (5-16%) of MeOH/DCM to give 1,4-dioxide 208 (56 mg, 53%) as an orange solid: mp 186-189° C.; 1H NMR δ 8.13 (t, J=1.6 Hz, 1H, H-9), 7.48 (br s, 2H, H-5, NH), 4.81 (t, J=8.3 Hz, 2H, H-7), 3.62 (t, J=6.0 Hz, 2H, CH2N), 3.37 (dt, J=8.3, 1.6 Hz, 2H, H-8), 2.62 (t, J=8.3 Hz, 2H, CH2N), 2.30 [s, 6H, N(CH3)2]; 13C NMR δ 167.2, 149.9, 140.6, 132.0, 117.9, 93.8, 87.9, 73.4, 57.5, 45.2 (2), 38.8, 28.5. HRMS (FAB+) calcd for C13H18N5O3 (MH+) m/z 292.1410, found 292.1409.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989451B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-535ba9e03a394550963efbce41f0b4e9 |
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| Source note | uspto-grants-2011_08 |
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