HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 178514602, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | HCID 178419719 | HCID 178419719 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178514602 | HCID 178514602 | 97% |
Reaction Steps
A mixture of 50 g (0.14 mol) of 2-bromo-1-(2-guanidino-4-thiazolyl)ethanone hydrobromide, 23.6 g (0.36 mol) of sodium azide, and 250 ml of dimethylformamide was stirred at room temperature for 1.5 hours. The mixture was poured into 1.5 liters of water, and the aqueous solution was made basic with solid sodium carbonate. The resulting precipitate was filtered, washed well with water, and dried, thereby affording 30.6 g (93%) of 2-azido-1-(2-guanidino-4-thiazolyl)-ethanone as a light brown crystalline solid, mp 177° (dec). Analytically pure material can be prepared by recrystallization from absolute ethanol: Calcd. for C6H7N7OS: C, 32.00; H, 3.13; N, 43.53; S. 14.24; found: C, 32.22; H, 3.43; N, 41.93; S, 13.97.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04510313 |
| Source dataset | uspto-grants-1985_04 |
| ORD ID | ord-088596ab0e184d6d8ede716aca7b14d3 |
| Source note | uspto-grants-1985_04 |