HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 13851189, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 13851173 | HCID 13851173 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 13851189 | HCID 13851189 | 100% |
Reaction Steps
A mixture of 5.8 parts of 7-amino-3-[4-[4-(4-fluorobenzoyl)-1-piperidinyl]butyl]-2,4(1H,3H)-quinazolinedione, 100 parts of acetic acid and 2.5 parts of acetic acid anhydride was stirred at reflux temperature. The reaction mixture was evaporated. The residue was stirred in water and ammonium hydroxide. The product was filtered off, washed with water and boiled in ethanol. After cooling, the product was filtered off, washed with 2,2'-oxybispropane and dried, yielding 6.3 parts (100%) of N-[3-[4-[4-(4-fluorobenzoyl)-1-piperidinyl]butyl]-1,2,3,4-tetrahydro-2,4-dioxo-7-quinazolinyl]-acetamide; mp. 273.1° C. (18).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04665075 |
| Source dataset | uspto-grants-1987_05 |
| ORD ID | ord-08561e07173949c49060e62b4fda5fe9 |
| Source note | uspto-grants-1987_05 |