Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Benzoic acid, 2-(isocyanatosulfonyl)-, methyl ester | HCID 156281 | — |
| Reactant | HCID 20435498 | HCID 20435498 | — |
| Product | HCID 13369444 | HCID 13369444 | — |
Reaction Steps
To a dry stirred solution of 0.5 g of 4,6-dimethylfuro[2,3-d]pyrimidin in 10 ml of acetonitrile at ambient temperature and pressure was added 1.6 g of 2-carbomethoxybenzenesulfonyl isocyanate. The resulting mixture was warmed on the steam bath for several minutes then stirred at ambient temperature for 4 hours. The suspended solid was collected by filtration and rinsed with acetonitrile to yield 0.87 g of methyl 2-{[(4,6-dimethylfuro[2,3-d]pyrimidin-2-yl)aminocarbonyl]aminosulfonyl}benzoate, m.p. 197°-198°. The product showed characteristic absorption bands at 1690 and 1735 cm-1 in the infrared spectrum and at 2.45, 2.75, 3.95, 6.6, 7.7, 8.3, 10.4 and 13.0 ppm in the nuclear magnetic resonance (60 MHz) spectrum indicating the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04487626 |
|---|
| Source dataset | uspto-grants-1984_12 |
|---|
| ORD ID | ord-f290c5549bd04ecfa5ec56a25c072f90 |
|---|
| Source note | uspto-grants-1984_12 |
|---|