HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 10342851, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | HCID 10072535 | HCID 10072535 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 10342851 | HCID 10342851 | — |
Reaction Steps
A mixture of 1.44 g of 8-(p-chlorophenylsulfonamido)-4-[3-(3-pyridyl)propyl]-octanamide (example 24) and 0.52 ml pyridine in 5.8 ml dioxane is cooled to 0° and 0.51 ml trifluoroacetic anhydride is added over a period of 1 h. The mixture is then stirred at room temperature for 3 h. The reaction is quenched by the addition of saturated aqueous sodium bicarbonate solution and extracted with methylene chloride (2×20 ml). The combined organic extracts are dried, filtered and evaporated to give 8-(p-chlorophenylsulfonamido)-4-[3-(3-pyridyl)propyl]-octanenitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05153214 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-ab80968b1f2548629422f5c1222fdb93 |
| Source note | uspto-grants-1992_10 |