HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 23471620, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 23471618 | HCID 23471618 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 23471620 | HCID 23471620 | — |
Reaction Steps
To a solution of 5-(5-methyl-3-oxo-2,3,4,5-tetrahydropyridazin-6-yl)indoline in 100 ml of chloroform was added 5 ml of triethylamine with stirring. To the mixture was added dropwise 3 ml of acetic anhydride. After maintaining at room temperature for one hour, the reaction mixture was concentrated under reduced pressure. The residual crystals were filtered off, washed with water and recrystallized from ethanol to give 4.3 g of 5-(5-methyl-3-oxo-2,3,4,5-tetrahydropyridazin-6-yl)-1-acetylindoline as white crystals, melting at 258°-261° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04258185 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-244f7a2d20454e34933c5944740d6b15 |
| Source note | uspto-grants-1981_03 |