HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-[Di-(tert-butoxycarbonyl)amino]methyl-7-nitro-2,3-dimethoxyquinoxaline → 5-Aminomethyl-2,3-dimethoxy-7-nitro-quinoxaline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-[Di-(tert-butoxycarbonyl)amino]methyl-7-nitro-2,3-dimethoxyquinoxaline | HCID 23298008 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 5-Aminomethyl-2,3-dimethoxy-7-nitro-quinoxaline | HCID 17915296 | — |
Reaction Steps
13.8 9 (29.7 mmol) of 5-[di-(tert-butoxycarbonyl)amino]methyl-7-nitro-2,3-dimethoxyquinoxaline are stirred at room temperature for 8 hours in 60 ml of trifluoroacetic acid. The reaction mixture is concentrated under reduced pressure and the red oil is well stirred at 0° for one hour with 1N potassium carbonate. The yellow crystals are filtered off, washed with 100 ml of water and 100 ml of a 1:1 mixture of ethyl acetate and hexane, and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06117873 |
| Source dataset | uspto-grants-2000_09 |
| ORD ID | ord-ceeffaaf095041cd815115f76703a569 |
| Source note | uspto-grants-2000_09 |