HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetoacetic Acid → HCID 178486676, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetoacetic Acid | HCID 96 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Isobutyryl chloride | HCID 62325 | — |
| Reactant | HCID 178486674 | HCID 178486674 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178486676 | HCID 178486676 | 39.4% |
Reaction Steps
4-Amino-3-hydroxy-6,7-dimethoxy-1-methylisoquinoline (BBQ) (1.772 grams, 5 mmol) as the diacetate solvate in 50 ml methylene chloride was treated with 2.5 ml triethylamine (16.5 mmol) for 5 minutes and subsequently with 0.63 ml isobutyryl chloride (6 mmol) with stirring under a nitrogen atmosphere. After 1 hour, the slurry was evaporated to dryness in vacuo and boiled in 50 ml methanol and 5 ml water for 15 minutes. The solid was isolated by filtration, washed successively with methanol and acetone, and then dried in vacuo at 50° C. to provide 0.6 grams of Compound BO (39.4% yield) having a melting point of 292°-294° C. (with decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04714705 |
| Source dataset | uspto-grants-1987_12 |
| ORD ID | ord-f6c0a230db7a4b09a9eac2d8cd7b61bb |
| Source note | uspto-grants-1987_12 |