HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclobutanone → 4-(4-((2-Cyanopropan-2-yl)amino)-2-fluorophenyl)butanenitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclobutanone | HCID 14496 | — |
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | 4-(4-Amino-2-fluorophenyl)butanenitrile | HCID 57672609 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-(4-((2-Cyanopropan-2-yl)amino)-2-fluorophenyl)butanenitrile | HCID 68734212 | 95.9% |
Reaction Steps
TMSCN (0.14 mL, 1.01 mmol) was added to a mixture of the compound 68 (60 mg, 0.34 mmol), cyclobutanone (0.15 mL, 2.04 mmol) and ZnCl2 (4 mg, 0.04 mmol) in dioxane (1 mL) with stirring. The reaction mixture was stirred at room temperature for 1 h, and concentrated in vacuo. The residue was diluted with water, and extracted with DCM. The combined organic layers were washed with brine, dried over Na2SO4 and concentrated to dryness to give compound 70 (80 mg, 91%) as a light yellow oil. The crude product was used directly for the next step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09216957B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-98eae07e7c6242a58aa77f98394f20dc |
| Source note | uspto-grants-2015_12 |