HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Dicyclohexylcarbodiimide → (R)-quinuclidin-3-yl 2-phenyl-2-(o-tolylamino)acetate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Edukt | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Edukt | 3-Quinuclidinol, (-)- | HCID 91404 | — |
| Edukt | Phenyl-o-methylphenylamino-acetic acid hydrochloride | HCID 67124826 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | (R)-quinuclidin-3-yl 2-phenyl-2-(o-tolylamino)acetate | HCID 46840573 | 103% |
Reaktionsschritte
PS-DCC (1.15 g, 1.44 mmol, loading: 1.25 mmol/g) was suspended in THF (15 ml). 2-Phenyl-2-(o-tolylamino)acetic acid hydrochloride (I22) (200 mg, 0.72 mmol) and HOBT (221 mg, 1.44 mmol) were added, followed by (R)-quinuclidin-3-ol (275 mg, 2.16 mmol), and the mixture was stirred for 16 hours at room temperature. PS-DCC was removed by filtration, and the filtrate was evaporated. The resulting residue was dissolved in EtOAc and washed sequentially with water, sat. NaHCO3, water and brine. The organic layer was dried over Na2SO4, filtered and evaporated to give the title compound (260 mg, quantitative yield, mixture of diastereomers).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08563577B2 |
| Quelldatensatz | uspto-grants-2013_10 |
| ORD ID | ord-d70e26e257bd4bc6922ebf2e9eb74833 |
| Quellennotiz | uspto-grants-2013_10 |