HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1365781Erstellt: 26. Oktober 2026
Iodine → 4-(5-Chloro-2-iodothiazolo[5,4-d]pyrimidin-7-yl)morpholine
https://huagongshe.com/reaction/1365781
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Iodine | HCID 807 | — |
| Edukt | 4-(5-Chlorothiazolo[5,4-d]pyrimidin-7-yl)morpholine | HCID 57685385 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 4-(5-Chloro-2-iodothiazolo[5,4-d]pyrimidin-7-yl)morpholine | HCID 25210284 | — |
Reaktionsschritte
To a solution of 4-(5-chlorothiazolo[5,4-d]pyrimidin-7-yl)morpholine 14 dissolved in THF at −78° C. was added 1.6M solution of n-butyllithium in hexanes). The reaction mixture was stirred at −78° C. for 30 minutes. A solution of iodine in THF was added and reaction mixture was allowed to slowly warm up to room temperature and stirred for 45 minutes. The reaction mixture was quenched with saturated aq. Na2S2O3, and extracted with dichloromethane. The combined organic layers were dried (Na2SO4) and concentrated. The crude reaction mixture was purified by flash chromatography to yield 4-(5-chloro-2-iodothiazolo[5,4-d]pyrimidin-7-yl)morpholine 18.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07893059B2 |
|---|
| Quelldatensatz | uspto-grants-2011_02 |
|---|
| ORD ID | ord-9d4b888d482e4e0bab634316bb35d1ed |
|---|
| Quellennotiz | uspto-grants-2011_02 |
|---|