HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 12822508, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | HCID 12822471 | HCID 12822471 | — |
| Solvent | Ethyl formate | HCID 8025 | — |
| Product | HCID 12822508 | HCID 12822508 | — |
Reaction Steps
A solution of N-[[3-(2-aminoethyl)-1H-indol-5-yl]methyl]methanesulphonamide (2.1 g) in ethanol (20 ml) and ethyl formate (25 ml) was refluxed for 17 h. The solvent was evaporated in vacuo and the residue was partitioned between sulphuric acid (1N; 100 ml) and ethyl acetate (150 ml). The aqueous layer was extracted with ethyl acetate (150 ml) and the combined organic extracts were washed with brine (50 ml) and potassium carbonate solution (15%; 50 ml) and dried (Na2SO4). Evaporation of the solvent in vacuo gave the crude product as a very viscous oil (2.2 g). The oil was dissolved in THF (8 ml), scratched and left overnight at room temperature. Filtration gave the title compound (1.3 g) as a white solid m.p. 121°-5°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04636521 |
| Source dataset | uspto-grants-1987_01 |
| ORD ID | ord-0ac6db0a320a4967ba188ab6e8030e40 |
| Source note | uspto-grants-1987_01 |