Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Tetraethyltin | HCID 11704 | — |
| Reactant | HCID 25139892 | HCID 25139892 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 25140184 | HCID 25140184 | 81% |
Reaction Steps
Pd(PPh3)4 (350 mg, 0.3 mmol) was added to a N2-purged, stirred solution of chloride 257 (750 mg, 3.0 mmol) and Et4Sn (1.2 mL, 6.0 mmol) in DME (35 mL), and the mixture was stirred at 85° C. for 18 h under N2. The solution was cooled to 20° C. and the solvent evaporated. The residue was purified by chromatography, eluting with a gradient (2-5%) of MeOH/DCM, to give 1-oxide 260 (590 mg, 81%) as a brown solid: mp 129-131° C.; 1H NMR δ 8.21 (s, 1H, H-10), 7.63 (s, 1H, H-5), 3.79 (s, 2H, H-6), 3.16 (t, J=6.0 Hz, 2H, H-8), 3.02 (q, J=7.6 Hz, 2H, CH2), 2.77 (t, J=6.0 Hz, 2H, H-9), 2.51 (s, 3H, NCH3), 1.43 (t, J=7.6 Hz, 3H, CH3); 13C NMR δ 167.3, 145.8144.6, 138.2, 131.7, 125.0, 118.8, 58.1, 52.3, 45.9, 30.7, 29.6, 12.2; MS (APCI) m/z 245 (MH+, 100%). Anal. calcd for C13H16N4O.¼H2O: C, 62.5; H, 6.7; N, 22.4. Found: C, 62.6; H, 6.6; N, 22.4%.
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-788bcf107b884e80ba164f4192080f28 |
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| Source note | uspto-grants-2011_08 |
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