HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Phenyl-1,3,8-triazaspiro(4.5)decan-4-one → 4-[5-(4-Oxo-1-phenyl-1,3,8-triazaspiro[4.5]-dec-8-ylmethyl)imidazol-1-ylmethyl]benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Phenyl-1,3,8-triazaspiro(4.5)decan-4-one | HCID 70556 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-((5-(Chloromethyl)-1H-imidazol-1-yl)methyl)benzonitrile hydrochloride | HCID 9795357 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-[5-(4-Oxo-1-phenyl-1,3,8-triazaspiro[4.5]-dec-8-ylmethyl)imidazol-1-ylmethyl]benzonitrile | HCID 9845380 | — |
Reaction Steps
A solution of 1-phenyl-1,3,8-triazaspiro[4.5]decan-4-one (230 mg, 1 mmol), 1-(4-cyanobenzyl)-5-chloromethylimidazole hydrochloride salt (265 mg, 1 mmol), and diisopropylethylamine (0.52 mL, 3 mmol) in anhydrous acetonitrile (5 mL) was stirred at room temp. for 2 days. The resulting mixture was concentrated under vacuum, and the residue was subjected to column chromatography on silica gel eluting with 5% methanol in ethyl acetate. The appropriate fractions were collected and concentrated. The residue was triturated with diethyl ether, and the white solid precipitated was collected by filtration to provide the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06172076B2 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-5f90ff147f054e1f99a6d5718902709b |
| Source note | uspto-grants-2001_01 |