HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → Phenyl (5-cyano-4-isopropoxypyridin-2-yl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | 6-Amino-4-isopropoxynicotinonitrile | HCID 118036970 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Phenyl (5-cyano-4-isopropoxypyridin-2-yl)carbamate | HCID 125470513 | — |
Reaction Steps
Phenyl chloroformate (3.89 ml, 31.0 mmol) was added drop wise to a mixture of 6-amino-4-isopropoxynicotinonitrile (intermediate 97, 2.5 g, 14.11 mmol) and pyridine (2.51 ml, 31.0 mmol) in THF (100 ml) at room temperature. The reaction mixture was stirred for 12 h at room temperature, additional pyridine (2.51 ml, 31.0 mmol) added, before stirring for an additional 12 h and then partitioned between EtOAc and saturated aqueous NaHCO3 solution. The organic layer was washed with saturated brine, dried over MgSO4 and evaporated. The residue was triturated with Et2O and the product obtained by filtration as a beige solid. (UPLC-MS 7) tR 1.09; ESI-MS 298.2 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09266883B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-c00926421b5b44e0871bb723bb874072 |
| Source note | uspto-grants-2016_02 |