Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | 1H-1-Benzazepine-2,5-dione, 3-methoxy- | HCID 10750663 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19704898 | HCID 19704898 | — |
Reaction Steps
3-Methoxy-2,5-dioxo-2,5-dihydro-1H-benz[b]azepine (0.5 g) and anhydrous lithium chloride (0.63 g) were added to dry tetrahydrofuran (10 mL), and the mixture was cooled to -70° C. To this was added diisopropylamine (380 mL), followed by butyllithium (2.2 mL, 2.5 M in hexanes); and the mixture was warmed to -20° C. After 30 minutes, methyl iodide (307 mL) was added and the mixture cooled to -10° C. for 10 minutes. The mixture was diluted with water, acidified with 2 N hydrochloric acid and extracted with ethyl acetate. The combined organic extracts were washed with brine, dried and evaporated. The solid was purified by chromatography, with ethyl acetate:toluene (1:1) as the eluent, and recrystallized from hot toluene to give the methylated product as a white solid (0.367 g); NHR: 2.03 (s,3); MS(EI): m/z=217(M).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05492905 |
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| Source dataset | uspto-grants-1996_02 |
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| ORD ID | ord-f2c0789e02274dc880e63c5a44c76e00 |
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| Source note | uspto-grants-1996_02 |
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