HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632200Generated: November 2, 2026
1,1'-Carbonyldiimidazole → HCID 178522697, compound
https://huagongshe.com/reaction/1632200
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | HCID 12763992 | HCID 12763992 | — |
| Reactant | HCID 178509299 | HCID 178509299 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178522697 | HCID 178522697 | 100.3% |
Reaction Steps
0.85 g (4 mmol) of imidazo-[1,2-a]-quinoline-2-carboxylic acid [prepared as in published French application No. 2,378,301] was heated at 160° C. in vacuo for one hour to remove water of crystallization and was then dissolved in 25 ml of dimethylformamide. The solution was stirred at 90° to 100° C. with 0.72 g (4.4 mmol) of carbonyldiimidazole and the mixture was stirred at 100° C. for 40 minutes to obtain a slight suspension. 0.375 g of anhydrous 5-amino-tetrazole were added to the mixture which was then stirred at 100° C. for 45 minutes and was then cooled to room temperature. 20 ml of ethyl acetate were added to the mixture and the mixture was cooled in ice and was filtered to obtain 1.12 g of N-(1H-tetrazol-5-yl)-imidazo-[1,2-a]-quinoline-2-carboxamide in the form of colorless crystals melting at 266°-268° C. after crystallization from dimethylformamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04474784 |
|---|
| Source dataset | uspto-grants-1984_10 |
|---|
| ORD ID | ord-5f7c18e197464e9bb2a5c4c0db7098d5 |
|---|
| Source note | uspto-grants-1984_10 |
|---|