HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 9-(1H-imidazol-1-yl)methyl-4-[(2-phenylethyl)amino]imidazo[5,1-h]pteridin-6(5H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4,6-Dichloro-5-nitropyrimidine | HCID 20312 | — |
| Reactant | Stannous Chloride | HCID 24479 | — |
| Reactant | N-Benzylphenethylamine | HCID 65055 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | HCID 178430886 | HCID 178430886 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | 9-(1H-imidazol-1-yl)methyl-4-[(2-phenylethyl)amino]imidazo[5,1-h]pteridin-6(5H)-one | HCID 9908192 | — |
Reaction Steps
Prepared by treatment of 4,6-dichloro-5-nitropyrimidine with N-benzylphenylethylamine, followed by reaction with 2-(1 H-imidazol-1 -yl)-methylimidazole, reduction with tin (II) chloride, cyclization with carbonyidiimidazole, and hydrogenation with palladium on carbon in ethanol containing 1.1 eq. NaOH at 50 psi and 50° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05854419 |
| Source dataset | uspto-grants-1998_12 |
| ORD ID | ord-880d68ea11b24ffcba43b4d3163d2f20 |
| Source note | uspto-grants-1998_12 |