HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Trifluoroacetic acid → Methyl (1R,3R)-1-(1,3-benzodioxol-5-yl)-2,3,4,9-tetrahydro-1H-pyrido(3,4-b)indole-3-carboxylate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Trifluoroacetic acid | HCID 6422 | — |
| Edukt | Piperonal | HCID 8438 | — |
| Edukt | Methyl D-Tryptophanate | HCID 168016 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Methyl (1R,3R)-1-(1,3-benzodioxol-5-yl)-2,3,4,9-tetrahydro-1H-pyrido(3,4-b)indole-3-carboxylate | HCID 10269318 | 36,8% |
Reaktionsschritte
To a stirred solution of D-tryptophan methyl ester (11 g) and piperonal (7.9 g) in anhydrous CH2Cl2 (400 mL) cooled at 0° C. was added dropwise trifluoroacetic acid (7.7 mL) and the solution was allowed to react at ambient temperature. After 4 days, the yellow solution was diluted with CH2Cl2 (200 mL) and washed with a saturated aqueous solution of NaHCO3, then with water (3×200 mL) and dried over Na2SO4. The organic layer was evaporated under reduced pressure and the residue containing the two geometric isomers was purified by flash chromatography eluting with dichloromethane/ethyl acetate (97/3) to give as the first eluting product the title compound (6.5 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06608065B1 |
| Quelldatensatz | uspto-grants-2003_08 |
| ORD ID | ord-538c62d37ba9478ab431af1e12fb68b8 |
| Quellennotiz | uspto-grants-2003_08 |