HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiazole → 2-cyano-N-(1,3-thiazol-2-yl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | Cyanoacetic acid | HCID 9740 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 2-cyano-N-(1,3-thiazol-2-yl)acetamide | HCID 693166 | — |
Reaction Steps
4.5 g of cyanoacetic acid and 5.3 g of 2-aminothiazole, each in acetonitrile were combined, and the suspension (60 ml) was treated with a solution of 12.0 g of dicyclohexylcarbodiimide in 30 ml of acetonitrile. After exothermic reaction (and solidification) additional acetonitrile (60 ml) was added and the mixture stirred 1 hr and let stand overnight. The collected solid (20 g) was stirred with dilute (ca. 2%) NaOH solution and filtered. The filtrate was acidified with 6 N HCl and the product collected, washed with water, dried (m.p. 229°-230°) and recrystallized from acetone to give 2-(cyanoacetylamino)thiazole, m.p. 231°-2° dec.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04435407 |
| Source dataset | uspto-grants-1984_03 |
| ORD ID | ord-7aed9a92fe354bd6b93832256714feb2 |
| Source note | uspto-grants-1984_03 |