HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxide → 2-Methyl-4-morpholino-5-fluoroindole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxide | HCID 961 | — |
| Reactant | 2-Methyl-4-morpholino-5-fluoro-7-bromoindole | HCID 20258993 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Methyl-4-morpholino-5-fluoroindole | HCID 20258992 | 65.7% |
Reaction Steps
To a solution of 24 g of 2-methyl-4-morpholino-5-fluoro-7-bromoindole in 200 ml of ethanol was added 1 g of palladium-carbon and then 15 ml of a 20% aqueous sodiium hydroxide solution. This mixture was subjected to catalytic reduction at room temperature and at atmospheric pressure. The reaction was stopped when a theoretical amount (about 1.7 l) of hydrogen was absorbed, and the catalyst was removed by filtration followed by concentration. The residue was purified through silica gel column chromatography (Wako gel C-200; eluent:chloroform:n-hexane=5:1) to give 11.8 g of 2-methyl-4-morpholino-5-fluoroindole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04399134 |
| Source dataset | uspto-grants-1983_08 |
| ORD ID | ord-f82e5e9786934fb2a560732e42ba15b4 |
| Source note | uspto-grants-1983_08 |