HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 7-(1-Ethyl-2-methylindol-3-yl)-7-(1,2-diphenylindolizin-3-yl)-5,7-dihydrofuro[3,4-b]pyridin-5-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 3-Pyridinecarboxylic acid, 2-((1-ethyl-2-methyl-1H-indol-3-yl)carbonyl)- | HCID 112344 | — |
| Reactant | 1,2-Diphenylindolizine | HCID 12747344 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 7-(1-Ethyl-2-methylindol-3-yl)-7-(1,2-diphenylindolizin-3-yl)-5,7-dihydrofuro[3,4-b]pyridin-5-one | HCID 20536954 | — |
Reaction Steps
A mixture of 1.6 grams of (1-ethyl-2-methylindol-3-yl) (3-carboxy-pyridin-2-yl)ketone, 1.85 grams of 1,2-diphenylindolizine and 10 ml. of acetic anhydride was heated at about 40° C. for 104 minutes and then cooled in an ice bath. The reaction mixture was filtered and the product was repeatedly recrystallized from a toluene-petroleum ether mixture until a constant melting point of 206.5°-207.5° C. was obtained. A chloroform solution of the final product produced a blue color when applied to a record sheet material coated with a zinc-modified phenolic resin.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04275206 |
| Source dataset | uspto-grants-1981_06 |
| ORD ID | ord-f1e1e6d530a844fb91e1cf1f62e263cc |
| Source note | uspto-grants-1981_06 |