HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-((S)-1-Amino-propyl)-5-fluoro-3-phenyl-3H-benzoimidazole-4-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | [(S)-1-(3-Cyano-4-fluoro-2-phenylaminophenylcarbamoyl)propyl]carbamic acid tert-butyl ester | HCID 68157031 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-((S)-1-Amino-propyl)-5-fluoro-3-phenyl-3H-benzoimidazole-4-carbonitrile | HCID 68157445 | 69.5% |
Reaction Steps
HCl in dioxane (4M, 10 mL, 0.04 mol) was added to a solution of [(S)-1-(3-cyano-4-fluoro-2-phenylaminophenylcarbamoyl)propyl]carbamic acid tert-butyl ester (0.54 g, 1.32 mmol) in dioxane (5 mL) at 20° C., and the resultant mixture stirred at 80° C. for 17 h. After cooling, the reaction mixture was partitioned between saturated aqueous NaHCO3 (20 mL) and EtOAc (3×20 mL). The combined EtOAc extracts were dried (Na2SO4) and concentrated in vacuo. The resulting residue was purified by chromatography (SiO2 0-20% methanol in EtOAc) to give the title compound as an oil (0.27 g, 69%) LCMS (method H): RT 2.03 min, [M+H]+ 295.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08653089B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-c697babf7dde4b28942bed0327461342 |
| Source note | uspto-grants-2014_02 |