HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfoxide → 3-{1-(2-naphtho[1,2-b]furan-3-yl-ethyl)-1,2,3,6-tetrahydro-4-pyridinyl}-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (1,2,3,6-tetrahydro-4-pyridinyl)-1H-indole | HCID 23001082 | — |
| Reactant | 3-(2-Iodo-ethyl)-naphtho[1,2-b]furan | HCID 23614451 | — |
| Product | 3-{1-(2-naphtho[1,2-b]furan-3-yl-ethyl)-1,2,3,6-tetrahydro-4-pyridinyl}-1H-indole | HCID 23614450 | — |
Reaction Steps
A mixture of 3-(2-iodo-ethyl)-naphtho[1,2-b]furan (321 mg. 1 mmol) (obtained by the above mentioned process) and 3 (1,2,3,6-tetrahydro-4-pyridinyl)-1H-indole (198 mg, 1 mmol) was heated at 120° C. in DMSO in the presence of N,N-diisopropylethylamine (5 ml, excess) for 24 hrs. At the end, the reaction mixture was quenched with water and extracted with chloroform. The organic layer was washed with water and dried over anhydrous MgSO4 and concentrated to dryness. The dark colored solid was purified by silica-gel column chromatography by eluting it with 70% ethyl acetate:hexane. 3-{1-(2-naphtho[1,2-b]furan-3-yl-ethyl)-1,2,3,6-tetrahydro-4-pyridinyl}-1H-indole was isolated as yellow solid. Yield: 120 mg (30%); 393 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07235569B2 |
| Source dataset | uspto-grants-2007_06 |
| ORD ID | ord-71d34400063241b78d77037b8deec5e5 |
| Source note | uspto-grants-2007_06 |