HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → (4R,9aR)-6-methoxy-4-methyl-3,4,9,9a-tetrahydro-1H-2,4a,5-triaza-fluorene-2-carboxylic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178418747 | HCID 178418747 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (4R,9aR)-6-methoxy-4-methyl-3,4,9,9a-tetrahydro-1H-2,4a,5-triaza-fluorene-2-carboxylic acid tert-butyl ester | HCID 69357234 | — |
Reaction Steps
To a solution of 0.25 g (0.82 mmol) (4R,9aR)-6-hydroxy-4-methyl-3,4,9,9a-tetrahydro-1H-2,4a,5-triaza-fluorene-2-carboxylic acid tert-butyl ester in 2 ml N,N-dimethylformamide, 40 mg (0.90 mmol) sodium hydride (55–65% dispersion in oil) was added. After 30 min, 0.10 ml (0.23 g, 1.64 mmol) methyl iodide was added. After 1 h the reaction mixture was poured onto water and extracted three times with ethyl acetate. The organic layers were washed twice with water, then brine and were dried over magnesium sulfate. After filtration and evaporation of the solvent the product was purified by column chromatography on silica gel (0.032–0.063 mm) with ethyl acetate:n-hexane (1:5) as eluant.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07098337B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-120c810d170145e48cb9f8656c3f06aa |
| Source note | uspto-grants-2006_08 |