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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 46124Erstellt: 23. Oktober 2026

3-Bromo-2-methyl-1-propene → HCID 178441184, Verbindung

https://huagongshe.com/de/reaction/46124

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Bromo-2-methyl-1-propeneHCID 357785—
EduktLithium diisopropylamideHCID 2724682—
EduktHCID 178518180HCID 178518180—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 178441184HCID 178441184—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To the mixture of 2-((1S,2S,4R)-bicyclo[2.2.1]heptan-2-ylamino)-5-(2-(tetrahydro-2H-pyran-2-yloxy)ethyl)thiazol-4(5H)-one (1160 mg, 3.43 mmol) in THF (8.0 mL) cooled in a −78° C. bath was added LDA (2.0 M, 17.15 mL). The resulting mixture was stirred for 10 min at −78° C., and then 3-bromo-2-methylprop-1-ene (1.6 ml, 17.15 mmol) was added. After the reaction mixture was allowed to warm to room temperature and stirred ca. 18 h. Saturated NaH2PO4 was added, and the aqueous phase was extracted with EtOAc. The organic layer was washed with sat'd NH4Cl, dried over MgSO4, filtered, and concentrated in vacuo. The crude residue was purified by flash chromatography (4:1; Hexane:EtOAc) to give the title compound as yellow oil. MS (ES+): 393 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08541592B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-a84efc7ef807409883ce185a741fb340
Quellennotizuspto-grants-2013_09