HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → ethyl 7-amino-1-(methoxymethyl)-1H-indole-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | ethyl 1-(methoxymethyl)-7-nitro-1H-indole-2-carboxylate | HCID 57475941 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | ethyl 7-amino-1-(methoxymethyl)-1H-indole-2-carboxylate | HCID 57475944 | 91.6% |
Reaction Steps
A mixture of ethyl 1-(methoxymethyl)-7-nitro-1H-indole-2-carboxylate (2.35 g), 10% palladium-carbon (0.24 g), ethanol (4 ml) and tetrahydrofuran (10 ml) was stirred overnight at room temperature under hydrogen atmosphere. The palladium-carbon was removed by filtration, and the filtrate was concentrated. The residue was subjected to silica gel column chromatography to give the title compound (1.92 g, yield 91%) as a yellow oil from a fraction eluted with ethyl acetate-hexane (1:3, volume ratio).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07777047B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-210b177eec414f9197c1f3f59cffadfb |
| Source note | uspto-grants-2010_08 |