HuagongsheHuagongshe Chemistry Print Report · For research reference only
Indole → 9-Methyl-6-triisopropylsilanyloxy-1,3,4,9-tetrahydro-beta-carboline-2-carboxylic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Indole | HCID 798 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | HCID 23544277 | HCID 23544277 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 9-Methyl-6-triisopropylsilanyloxy-1,3,4,9-tetrahydro-beta-carboline-2-carboxylic acid tert-butyl ester | HCID 23544276 | 41.9% |
Reaction Steps
A solution of 6-triisopropylsilanyloxy-1,3,4,9-tetrahydro-β-carboline-2-carboxylic acid tert-butyl ester (175 mg, 0.39 mmol) in 3 mL of ethyl ether was added to a vigorously stirring solution of potassium tert-butoxide (263 mg) and 18-crown-6 (16 mg) in 10 mL ethyl ether. After 10 min, iodomethane (73 uL) in 0.5 mL of ethyl ether was added to the indole solution and the resulting mixture was stirred for 2 h. The solids were removed by filtration and the solvent was evaporated. Silica gel chromatography (10% ethyl acetate in hexanes) gave 9-methyl-6-triisopropylsilanyloxy-1,3,4,9-tetrahydro-β-carboline-2-carboxylic acid tert-butyl ester (75 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07084154B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-b5ef23cd1e7d40e5b80f3c58363f7221 |
| Source note | uspto-grants-2006_08 |