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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071889Generated: October 30, 2026

4-Diazo-4H-imidazole-5-carboxamide → HCID 178449900, compound

https://huagongshe.com/reaction/2071889

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Diazo-4H-imidazole-5-carboxamideHCID 53426585—
ReactantHCID 178449087HCID 178449087—
SolventEthanolHCID 702—
ProductHCID 178449900HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04049639
Source datasetuspto-grants-1977_09
ORD IDord-7b7a1c6dc53c4518a54c5d58e87db2a6
Source noteuspto-grants-1977_09