HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1187367Generated: October 29, 2026
Tetrahydrofuran → 6-chloro-N-cyclohexyl-2-[2-(4-fluorophenyl)ethoxy]nicotinamide
https://huagongshe.com/reaction/1187367
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 4-Fluorophenethyl Alcohol | HCID 82068 | — |
| Reactant | 2,6-dichloro-N-cyclohexylnicotinamide | HCID 52762493 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 6-chloro-N-cyclohexyl-2-[2-(4-fluorophenyl)ethoxy]nicotinamide | HCID 59830681 | 40.6% |
Reaction Steps
2,6-dichloro-N-cyclohexylnicotinamide (Intermediate 1, 273 mg, 1 mmol) was stirred in 1,4-dioxane (4 ml). To this solution was added 4-fluorophenethyl alcohol (154 mg, 1.1 mmol) followed by bis-sodium hexamethyldisilylamide 1.0M in THF (1.1 ml, 1.1 mmol). The tube was sealed and subjected to microwave heating 150° C. (Biotage Initiator 300 W) for 2 hours. The solvent was evaporated and the residue was diluted with water (15 ml) and extracted with dichloromethane (2×20 ml). The combined extract was washed with brine (20 ml) dried over MgSO4, filtered and evaporated. The crude product was purified on SiO2 (40 g) eluting with ethyl acetate/isohexane 0-40% and gave 6-chloro-N-cyclohexyl-2-[2-(4-fluorophenyl)ethoxy]nicotinamide (153 mg, 40%) as a white solid
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08673938B2 |
|---|
| Source dataset | uspto-grants-2014_03 |
|---|
| ORD ID | ord-4e93512bae9640d5acd6a18aef349882 |
|---|
| Source note | uspto-grants-2014_03 |
|---|