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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 473953Erstellt: 25. Oktober 2026

Diisopropyl diazene-1,2-dicarboxylate → Methyl 3-(5-bromopyridin-2-yloxy)cyclopentane carboxylate

https://huagongshe.com/reaction/473953

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
EduktCyclopentanecarboxylic acid, 3-hydroxy-, methyl esterHCID 520596—
EduktHCID 178515818HCID 178515818—
LösungsmittelTolueneHCID 1140—
ProduktMethyl 3-(5-bromopyridin-2-yloxy)cyclopentane carboxylateHCID 5857790751%

Reaktionsschritte

A solution of methyl 3-hydroxycyclopentanecarboxylate A-11 (500.0 mg, 3.00 mmol) in anhydrous toluene (10.0 mL) was added to a solution of 5-bromopyridin-2-ol (522.0 mg, 3.00 mmol) in anhydrous toluene (10.0 mL) at room temperature. Diisopropyl azodicarboxylate (1.57 g, 6.00 mmol) was then added dropwise, and the yellow-orange solution was stirred at room temperature for 12 h. The reaction mixture was then quenched with methanol (1.0 mL) and concentrated to dryness under reduced pressure. The residue was purified by flash column chromatography on silica gel (hexanes to ethyl acetate gradient) to give methyl 3-(5-bromopyridin-2-yloxy)cyclopentane carboxylate A-12 (462.0 mg, Yield=51%). MS (ESI), [M+Na]+ 321, 323.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08637507B2
Quelldatensatzuspto-grants-2014_01
ORD IDord-9b2e0014adbe449db1634b351e2ff97b
Quellennotizuspto-grants-2014_01