HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-2,3-dimethylbutanamide → 6-[(1-Carbamoyl-1,2-dimethylpropyl)carbamoyl]furo[2,3-b]pyridine-5-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-2,3-dimethylbutanamide | HCID 9793773 | — |
| Reactant | Furo[2,3-b]pryidine-5,6-Dicarboxylic anhydride | HCID 13752513 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-[(1-Carbamoyl-1,2-dimethylpropyl)carbamoyl]furo[2,3-b]pyridine-5-carboxylic acid | HCID 13752514 | 97.9% |
Reaction Steps
2-Amino-2,3-dimethylbutyramide (2.1 g, 0.016 mol) is added to a stirred suspension of furo[2,3-b]pyridine-5,6-dicarboxylic acid anhydride (3.0 g, 0.016 mol) in tetrahydrofuran (7.5 mL) and the mixture allowed to stir at room temperature for 16 hours. The reaction mixture is then stirred at 60° C. for one hour, cooled to room temperature, either added, and the solid filtered off and dried to give 5 g of 6-[(1-carbamoyl-1,2-dimethylpropyl)carbamoyl]furo[2,3-b]pyridine-5-carboxylic acid mp 192°-196° C. (dec).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04752323 |
| Source dataset | uspto-grants-1988_06 |
| ORD ID | ord-7535937d28fd4c95929950089c44a72c |
| Source note | uspto-grants-1988_06 |