HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 6-Bromo-2a-[4-(2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-2-yl)-butyl]-2a,3,4,5-tetrahydro-1H-benz[cd]indol-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Tetrahydro-beta-carboline | HCID 107838 | — |
| Reactant | 6-Bromo-2a-(4-bromobutyl)-2a,3,4,5-tetrahydrobenz[cd]indole-2(1H)-one | HCID 10981946 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Bromo-2a-[4-(2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-2-yl)-butyl]-2a,3,4,5-tetrahydro-1H-benz[cd]indol-2-one | HCID 18377354 | 70% |
Reaction Steps
A 31 mg (0.18 mmol) portion of 2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole and 62 mg (0.54 mmol) of potassium carbonate were added to 1 ml of DMF solution containing 58 mg (0.15 mmol) of 6-bromo-2a-(4-bromobutyl)-2a,3,4,5-tetrahydro-1H-benz[cd]indol-2-one and stirred overnight at room temperature. The reaction solution was extracted with ethyl acetate and washed with water. After drying (Na2SO4), the solvent was removed by evaporation under a reduced pressure and the residue was recrystallized from acetone-diisopropyl ether to obtain 50 mg of the title compound (70% in yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06498251B1 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-5601c5bb63af4f0c9829a0fd45803501 |
| Source note | uspto-grants-2002_12 |