HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 1-(4-Chlorobenzyl)-3-(2-(3-pyridyl)ethenyl)-5-(2-quinolylmethoxy)indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 19097338 | HCID 19097338 | — |
| Reactant | Triphenyl(3-pyridylmethyl)phosphonium chloride | HCID 22325077 | — |
| Solvent | Water ethylacetate | HCID 22728543 | — |
| Product | 1-(4-Chlorobenzyl)-3-(2-(3-pyridyl)ethenyl)-5-(2-quinolylmethoxy)indole | HCID 54501102 | 30.5% |
Reaction Steps
A suspension of sodium hydride (60%-oil suspension, 0.39 g), 3-picolyl-triphenylphosphonium chloride (2.55 g) and N,N-dimethylformamide was stirred for 20 minutes, followed by the addition of 1-(4-chlorobenzyl)-3-formyl-5-(2-quinolylmethoxy)indole (3.0 g). The mixture was stirred for an additional 10 hours and then poured into water-ethyl acetate (50% v/v). The organic layer was separated, washed with brine, dried over magnesium sulfate, and concentrated in vacuo. The resultant crude product was purified by chromatography on silica gel using 50%-ethyl acetate in n-hexanes as eluent to yield 1-(4-chlorobenzyl)-3-(2-(3-pyridyl)ethenyl)-5-(2-quinolylmethoxy)indole (1.0 g), m.p. 169°-171° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05290788 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-6430d7dc8c0b4b4dba5c96136a706f3d |
| Source note | uspto-grants-1994_03 |