HuagongsheHuagongshe Chemistry Print Report · For research reference only
Amantadine → HCID 70569991, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Amantadine | HCID 2130 | — |
| Reactant | 1-AMINOADAMATANE, 3-METHYL | HCID 3010128 | — |
| Reactant | HCID 20289894 | HCID 20289894 | — |
| Product | HCID 70569991 | HCID 70569991 | — |
Reaction Steps
Following the above procedure, but substituting 3-methyl-1-adamantylamine for 1-adamantylamine, there was prepared a salt of 6,7-dibromo-3,4-dihydro-3-oxo-2-quinoxaline carboxylic acid and 3-methyl-1-adamantylamine. The crystalline product was isolated by filtration and dried; melting point=280°-282° C. with decomposition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04252954 |
| Source dataset | uspto-grants-1981_02 |
| ORD ID | ord-94e225098f2148d1b2c08290d69fc0f6 |
| Source note | uspto-grants-1981_02 |