HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formic Acid → HCID 14456844, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 19854390 | HCID 19854390 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14456844 | HCID 14456844 | — |
Reaction Steps
On the other hand, 5.52 g of formic acid is added to 12.25 g of acetic anhydride at room temperature and the mixture is stirred at 45°-50° C. for 1 hour. After cooling, 60 ml of tetrahydrofuran and 5.83 g of the above-prepared crystals of 6-(2-aminoethylthio)imidazo[1,2-b]pyridazine are added and the mixture is stirred at room temperature for 1 hour. The solvent is distilled off under reduced pressure and the residue made basic with a saturated aqueous solution of sodium hydrogen carbonate. The precipitated crystals are collected by filtration to give 2.83 g of 6-(2-formylaminoethylthio)imidazo[1,2-b]pyridazine as colorless crystals melting at 148° to 151° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04921851 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-aeea2949822c4c6999d04bb31596ac29 |
| Source note | uspto-grants-1990_05 |