HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiourea → 5-(Pyrimid-5-ylmethyl)-2-thiouracil
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Ethyl 2-formyl-3-(5-pyrimidyl)propionate | HCID 21936283 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-(Pyrimid-5-ylmethyl)-2-thiouracil | HCID 10966039 | 33.7% |
Reaction Steps
Sodium (0.25 g) was dissolved in ethanol (5 ml), thiourea (0.77 g) added, and the mixture stirred under reflux for 1 hour. A solution of ethyl 2-formyl-3-(5-pyrimidyl)propionate (1.99 g) in ethanol (5 ml) was added slowly, and reflux continued for 18 hours. The solvent was evaporated, and the residue taken up in water and washed with dichloromethane. The aqueous solution was acidified to pH 5, and the precipitate filtered off, washed with water and dried to obtain 5-(pyrimid-5-ylmethyl)-2-thiouracil (0.71 g). 1H-NMR (d6-DMSO) δ3.58 (2H,s), 7.54 (1H,s), 8.70 (2H,s) and 9.02 (1H,s). MPt 265-6° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06953803B1 |
| Source dataset | uspto-grants-2005_10 |
| ORD ID | ord-03bc384f19014d45bf29f0edc9e8d8cf |
| Source note | uspto-grants-2005_10 |