HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N-[[(4-fluorophenyl)carbamoyl]amino]-1,2,3,6-tetrahydropyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | N-[[(4-fluorophenyl)carbamoyl]-imino]pyridinium | HCID 20152379 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-[[(4-fluorophenyl)carbamoyl]amino]-1,2,3,6-tetrahydropyridine | HCID 13534699 | — |
Reaction Steps
A suspension of N-[[(4-fluorophenyl)carbamoyl]-imino]pyridinium ylide (1.04 g) and sodium borohydride (2.55 g) in ethanol (100 ml) was stirred at ambient temperature for 16 hours. Excess of sodium borohydride was decomposed with water, and the resulting mixture was evaporated. The residue was extracted with chloroform (20 ml×3). The combined organic extract was washed with water, dried over magnesium sulfate and evaporated to give crystalls. Recrystallization from diisopropyl ether gave N-[[(4-fluorophenyl)-carbamoyl]amino]-1,2,3,6-tetrahydropyridine (0.60 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04725608 |
| Source dataset | uspto-grants-1988_02 |
| ORD ID | ord-ba8e9518e9a14e998c41606e7292d98b |
| Source note | uspto-grants-1988_02 |