HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(2-Hydroxyethyl)piperazine → 5-(4'phenoxyphenyl)-5-[N-(2-hydroxyethyl)piperazinyl]barbituric acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(2-Hydroxyethyl)piperazine | HCID 7677 | — |
| Reactant | 5-Bromo-5-(4'-phenoxyphenyl)barbituric acid | HCID 22732233 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-(4'phenoxyphenyl)-5-[N-(2-hydroxyethyl)piperazinyl]barbituric acid | HCID 18408829 | 75.3% |
Reaction Steps
A solution of 5-Bromo-5-(4′-phenoxyphenyl)barbituric Acid (50 mg) in 0.2 ml of methanol is added dropwise with a solution of N-(2-hydroxyethyl)piperazine (52 mg) in 0.6 ml of methanol and the mixture is stirred for 2 hours. The white precipitate is recovered by filtration and dried under vacuum at 60° C. overnight. 42.6 mg of the product are obtained, m.p. >240° C. 1H-NMR in d6-DMSO: 2.2-2.45 ppm (m, 6H); 2.55 ppm (m, 4H); 3.45 ppm (m, 2H); 4.4 ppm (t, 1H); 6.9-7.7 ppm (m, 9H); 11.6 ppm (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06472396B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-460ab6e0218a4e3a867abe07986866ed |
| Source note | uspto-grants-2002_10 |