HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Diazo-4H-imidazole-5-carboxamide → HCID 178449900, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Diazo-4H-imidazole-5-carboxamide | HCID 53426585 | — |
| Reactant | HCID 178449087 | HCID 178449087 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178449900 | HCID 178449900 | — |
Reaction Steps
1.2 g. of N-butyl-acetamidine (Bp.: 76°-78° C./0.4 torr) are dissolved in 50 ml of anhydrous ethanol, whereafter 1.4 g. of 5-diazo-imidazole-4-carboxamide are added at 25° C. under stirring within 10 minutes. After 2.5 hours the orange-colored solution is clarified with activated characoal and evaporated in vacuo. 2.6 g. of a slowly crystallizing resin are obtained, which is twice crystallized from an ethanol-acetone mixture. Thus, a colorless, crystalline product, the 5-[3-n-butyl-3-(alpha-iminoethyl)-1-triazeno]-imidazole-4-carboxamide, melting at 191° C., is obtained (decomposition)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04049639 |
| Source dataset | uspto-grants-1977_09 |
| ORD ID | ord-7b7a1c6dc53c4518a54c5d58e87db2a6 |
| Source note | uspto-grants-1977_09 |