HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2169184Erstellt: 27. Oktober 2026
Phosphorus oxychloride → HCID 178464493, Verbindung
https://huagongshe.com/reaction/2169184
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Phosphorus oxychloride | HCID 24813 | — |
| Edukt | Dry ice ethyleneglycol | HCID 86601574 | — |
| Edukt | N-(2-(tert-butyldimethylsilyloxy)ethyl)-1,1,1-trifluoropropan-2-amine | HCID 86725834 | — |
| Edukt | HCID 178524871 | HCID 178524871 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Produkt | HCID 178464493 | HCID 178464493 | 58,3% |
Reaktionsschritte
To a solution of 5-(benzyloxy)-2-((1-(4-chlorophenyl)cyclopentyl)methyl)-6-hydroxypyrimidine-4-carboxylic acid (28-02) (150 mg, 342 μmol, Eq: 1.00) and N-(2-(tert-butyldimethylsilyloxy)ethyl)-1,1,1-trifluoropropan-2-amine (41) (102 mg, 376 μmol, Eq: 1.1) in pyridine (1.5 ml) was added POCl3 (157 mg, 95.6 μl, 1.03 mmol, Eq: 3.00) at −10° C. (ethylene glycol-dry-ice bath), then the reaction mixture was stirred at 0° C. for 2 hr. Ice cooled-water was slowly added to the reaction mixture at 0° C., which was extracted with ethyl acetate. The organic layer was washed with aqueous saturated NaHCO3 solution, dried (MgSO4), concentrated, and chromatographed (silica gel, gradient 5 to 50% ethyl acetate-hexane) to obtain 5-(benzyloxy)-N-(2-(tert-butyldimethylsilyloxy)ethyl)-2-((1-(4-chlorophenyl)cyclopentyl)methyl)-6-hydroxy-N-(1,1,1-trifluoropropan-2-yl)pyrimidine-4-carboxamide (42) (oil, 138 mg, 199 μmol, 58.3% yield).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US09045486B2 |
|---|
| Quelldatensatz | uspto-grants-2015_06 |
|---|
| ORD ID | ord-afe21fbb8ac64f81b1509f78d6360f15 |
|---|
| Quellennotiz | uspto-grants-2015_06 |
|---|