Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | HCID 25139892 | HCID 25139892 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 25139025 | HCID 25139025 | 88.7% |
Reaction Steps
A solution of chloride 257 (500 mg, 2.0 mmol) and ethylamine (0.4 mL, 6.0 mmol) in DME (15 mL) was heated at 60° C. for 4 h in a sealed pressure tube. The solution was cooled to 20° C., the solid filtered off and solvent evaporated. The combined residue was purified by chromatography, eluting with a gradient (2-4%) of MeOH/DCM, to give 1-oxide 258 (460 mg, 88%) as a yellow solid: mp 193-196° C.; 1H NMR δ 8.03 (s, 1H, H-10), 7.27 (s, 1H, H-5), 5.07 (br s, 1H, NH), 3.69 (s, 2H, H-6), 3.53 (dq, J=7.2, 5.8 Hz, 2H, CH2N), 3.05 (t, J=6.0 Hz, 2H, H-8), 2.72 (t, J=6.0 Hz, 2H, H-9), 2.48 (s, 3H, NCH3), 1.29 (t, J=7.2 Hz, 3H, CH3); 13C NMR δ 158.6, 147.0, 144.4, 132.5, 129.6, 122.8, 119.3, 58.2, 52.6, 46.0, 36.3, 29.1, 14.8; MS (APCI) m/z 260 (MH+, 100%). Anal. calcd for C13H17N5O: C, 60.2; H, 6.6; N, 27.0. Found: C, 59.9; H, 6.6; N, 26.9%.
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-c8af2f4003a5447d8361d77ae6d9a768 |
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| Source note | uspto-grants-2011_08 |
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