HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 6-Amino-4-methyl-beta-carboline-3-carboxylic-acid-ethylester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 4-Methyl-6-nitro-beta-carbolin-3-carboxylic acid ethyl ester | HCID 13037336 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-Amino-4-methyl-beta-carboline-3-carboxylic-acid-ethylester | HCID 13037338 | 88.9% |
Reaction Steps
1.02 g of 4-methyl-6-nitro-β-carbolin-3-carboxylic acid ethyl ester is dissolved or suspended in 30 ml of ethanol and 6 ml of tetrahydrofuran and, after the addition of 150 ml of palladium-carbon (10%), is hydrogenated at 24° C. and normal pressure. Within 3.5 hours, 210 ml of hydrogen is absorbed. The solution is filtered off and the catalyst and the solvent is distilled off in vacuo. The crude product is recrystallized from methanol-chloroform. 816 mg of 6-amino-4-methyl-β-carbolin-3-carboxylic acid ethyl ester of melting point 225°-238° C. (decomposition) is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05010077 |
| Source dataset | uspto-grants-1991_04 |
| ORD ID | ord-cc63fabfe0d3425bb62c6a0fa6ded733 |
| Source note | uspto-grants-1991_04 |