HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Potassium hydroxide ethanol → 2-Amino-3-hydroxy-3-(pyridin-4-yl)-1-(pyrrolidin-1-yl)propan-1-one, (2R,3S)-
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Potassium hydroxide ethanol | HCID 21946426 | — |
| Edukt | (-)-(2R,3S)-2-Amino-3-hydroxy-3-pyridin-4-yl-1-pyrrolidin-1-yl-propan-1-one di-p-toluoyl-L-tartrate | HCID 131734560 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Produkt | 2-Amino-3-hydroxy-3-(pyridin-4-yl)-1-(pyrrolidin-1-yl)propan-1-one, (2R,3S)- | HCID 11535990 | — |
Reaktionsschritte
Step 3 contains three sub-steps. In step 3a, the (−)-(2R,3S)-2-Amino-3-hydroxy-3-pyridin-4-yl-1-pyrrolidin-1-yl-propan-1-one di-p-toluoyl-L-tartrate (ON-PYRAMIDE DPTL Tartrate) is treated with aqueous KOH/Ethanol and acetone to give the corresponding free base, i.e., (−)-(2R,3S)-2-Amino-3-hydroxy-3-pyridin-4-yl-1-pyrrolidin-1-yl-propan-1-one (ON-PYRAMID free base). Following this, there is a resin treatment with a sulfonic resin. Finally, tartrate formation takes place by treatment of the free base with L-tartaric acid in the presence of denatured ethanol. The detailed manufacturing process is given below:
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US09242935B2 |
| Quelldatensatz | uspto-grants-2016_01 |
| ORD ID | ord-b19c5cd52f4c4e6b9fc20bebcef258e8 |
| Quellennotiz | uspto-grants-2016_01 |