HuagongsheHuagongshe Chemistry Print Report · For research reference only
Quinoxaline-2-carboxylic acid → N-{4-[4-amino-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-1-yl]butyl}quinoxaline-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Quinoxaline-2-carboxylic acid | HCID 96695 | — |
| Reactant | 1-(4-aminobutyl)-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-4-amine | HCID 22180872 | — |
| Product | N-{4-[4-amino-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-1-yl]butyl}quinoxaline-2-carboxamide | HCID 10322446 | 12% |
Reaction Steps
Using the general method of Example 181 1-(4-aminobutyl)-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-4-amine (1.5 g, 4.78 mmol) was reacted with 2-quinoxalinecarboxylic acid (1.0 g, 5.74 mmol) to provide 270 mg of N-{4-[4-amino-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-1-yl]butyl}quinoxaline-2-carboxamide as a yellow crystalline solid, m.p. 85-87° C. Analysis: Calculated for C26H27N7O2: % C, 66.51; % H, 5.80; % N, 20.88. Found: % C, 66.12; % H, 5.70; % N, 20.62.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06756382B2 |
| Source dataset | uspto-grants-2004_06 |
| ORD ID | ord-6fe36ff6a92b4d5ab4218f4106bb4903 |
| Source note | uspto-grants-2004_06 |