HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 20300066, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 3-Pyridinecarboxylic acid, 2-((1-ethyl-2-methyl-1H-indol-3-yl)carbonyl)- | HCID 112344 | — |
| Reactant | 6-(4-Methoxyphenyl)imidazo[2,1-b]thiazole | HCID 369507 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 20300066 | HCID 20300066 | 123.6% |
Reaction Steps
A mixture of 0.92 gram of 6-p-methoxy phenylimidazo[2,1-b]thiazole, 0.69 gram of (1-ethyl-2-methylindol-3-yl)(3-carboxypyridin-2-yl)ketone and 20 ml. of acetic anhydride was stirred 2.5 hours at 50° C. The reaction solution was poured into 250 ml. of water and adjusted to pH 9.8 with ammonium hydroxide. After one hour stirring the solid material was filtered and washed with water to give 1.44 grams (95%) of desired product, mp. 115°-118° C. The infrared spectrum showed a strong 1770 cm-1 lactone carbonyl peak. A solution of the product on silica gel produced a purple color.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04242513 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-4b1c835a998f463aafd6d4f2241a8553 |
| Source note | uspto-grants-1980_12 |