HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenobarbital → HCID 19975187, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenobarbital | HCID 4763 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-Bromovaleric acid | HCID 16368 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 19975187 | HCID 19975187 | — |
Reaction Steps
The DppE amide of 1-(4-carboxybutyl)-5-ethyl-5-phenyl barbituric acid (DPPE-phenobarbital) was prepared as outlined in FIG. 2. The sodium salt of phenobarbital (compound A) (2 mmoles) formed by treating phenobarbital with sodium hydroxide was reacted with the methyl ester of 5-bromovaleric acid (2.200 mmoles) in 5 ml of N,N-dimethyl formamide, for 4 hrs at 96° C., to form the methyl ester of 1-(4-carboxybutyl)-5-ethyl-5-phenyl barbiturate (compound B). The product was purified by column chromatography at a yield of about 77%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04783400 |
| Source dataset | uspto-grants-1988_11 |
| ORD ID | ord-8e77c1501bf44873af67467412e177b3 |
| Source note | uspto-grants-1988_11 |