HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propyl mercaptan → 3-Butyl-6-propylthio-1-[[2'-(N-trityltetrazol-5-yl)biphenyl-4-yl]methyl]pyrimidine-2,4(1H,3H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propyl mercaptan | HCID 7848 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-butyl-6-chloro-1-[[2'-(N-trityltetrazol-5-yl)biphenyl-4-yl]methyl]pyrimidine-2,4(1H,3H)-dione | HCID 19811529 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-Butyl-6-propylthio-1-[[2'-(N-trityltetrazol-5-yl)biphenyl-4-yl]methyl]pyrimidine-2,4(1H,3H)-dione | HCID 19811524 | 68% |
Reaction Steps
A mixture of 3-butyl-6-chloro-1-[[2'-(N-trityltetrazol-5-yl)biphenyl-4-yl]methyl]pyrimidine-2,4(1H,3H)-dione (1.4 g), propylmercaptan (0.24 ml) and potassium carbonate (0.35 g) in acetonitrile (25 ml) was heated under reflux for 3 hours. The reaction mixture was allowed to cool and the precipitate was removed by filtration. The filtrate was concentrated to dryness. The resulting residue was purified by column chromatography on silica gel to give colorless amorphous powders (1 g, 68%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05162326 |
| Source dataset | uspto-grants-1992_11 |
| ORD ID | ord-64d9b91b276448b792406ed2a94d7722 |
| Source note | uspto-grants-1992_11 |