HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → HCID 22491695, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | p-Chlorophenacyl bromide | HCID 68303 | — |
| Reactant | HCID 178508933 | HCID 178508933 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22491695 | HCID 22491695 | 72% |
Reaction Steps
A solution of 1.4 g (6.22 mmol) acyclovir, 30 mL DMF, and 400 mg sodium hydride (80%) was stirred at room temperature for 30 min, then 0.7 mL 2-bromo-4′-chloroacetophenone was added dropwise into the solution. Changing to orange color, the solution was added 17 mL ammonia, and continuously stirred for 5 hr. The solvent was removed to obtain a residue, which was washed with water. The product, 3-(2-hydroxy-ethoxymethyl)-6-(4-chlorophenyl)-3,5-dihydro-1,3,4,5,7a-pentaaza-s-indacen-8-one, was produced and weighted 1.62 g (white solid, yield 72%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06887997B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-363283d716334c30af74de79a9d9ffa7 |
| Source note | uspto-grants-2005_05 |