HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl isothiocyanatoformate → 3-[(6-Phenoxypyridin-3-yl)methyl]-2-thioxo-1,2,3,7-tetrahydro-6H-purin-6-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl isothiocyanatoformate | HCID 85320 | — |
| Reactant | 4-{[(6-Phenoxypyridin-3-yl)methyl]amino}-1H-imidazole-5-carboxamide | HCID 67414931 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-[(6-Phenoxypyridin-3-yl)methyl]-2-thioxo-1,2,3,7-tetrahydro-6H-purin-6-one | HCID 24855631 | 12.3% |
Reaction Steps
Ethoxycarbonyl isothiocyanate (0.096 mL, 0.85 mmol) was added to 4-{[(6-phenoxypyridin-3-yl)methyl]amino}-1H-imidazole-5-carboxamide (0.25 g, 0.81 mmol, obtained from Example 25(a)) in anhydrous dichloromethane (3.0 mL). After stirring for 2.5 h at ambient temperature the mixture was concentrated to dryness. Sodium hydroxide (10 mL, 2% w/v) was added and the solution was heated at 50° C. over night. After cooling, the pH was adjusted to 4-5 using 2N HCl. The solid was collected by filtration and recrystallized from DMSO/water to give a white crystalline material. A portion of this material was recrystallized from MeOH to give 35 mg (0.10 mmol, 12% yield) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08026244B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-2591b12836e44902b78838ed8eebe95f |
| Source note | uspto-grants-2011_09 |