HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Malonate → (+/-)-Ethyl 8-bromo-1-(2-ethoxy-2-oxoethyl)-6-fluoro-3-oxo-2,3-dihydro-1h-pyrrolo[1,2-a]indole-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | ethyl-3-(4-bromo-6-fluoro-1H-indol-2-yl)prop-2-enoate | HCID 69561024 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (+/-)-Ethyl 8-bromo-1-(2-ethoxy-2-oxoethyl)-6-fluoro-3-oxo-2,3-dihydro-1h-pyrrolo[1,2-a]indole-2-carboxylate | HCID 91021522 | 89.4% |
Reaction Steps
To a solution of diethyl malonate (1.67 g, 10.4 mmol) in EtOH (30 mL) at r.t. was added sodium methoxide (2.26 mL, 25% solution in MeOH). The mixture was stirred for 5 minutes and a solution of the compound of Step 3 (1.3 g, 4.2 mmol) in EtOH (10 mL) was added. The mixture was stirred at 75° C. for 12 hours, saturated aqueous NH4Cl was added and the aqueous layer was extracted with EtOAc. The combined organic layers were dried over Na2SO4 and concentrated. The residue was purified by silica gel chromatography eluted with 20% EtOAc to give 1.6 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07144913B2 |
| Source dataset | uspto-grants-2006_12 |
| ORD ID | ord-788d03ed6a9f4e1f99f937b6413ae2fa |
| Source note | uspto-grants-2006_12 |