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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1521708Erstellt: 25. Oktober 2026

Sodium hydride → HCID 67238426, Verbindung

https://huagongshe.com/reaction/1521708

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
EduktDiethyl 1H-pyrrolo[2,3-B]pyridine-2,6-dicarboxylateHCID 67236396—
EduktTert-butyl 6-methyl-1,2,3-oxathiazinane-3-carboxylate 2,2-dioxideHCID 86682388—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 67238426HCID 6723842673%

Reaktionsschritte

To a solution of diethyl 1H-pyrrolo[2,3-b]pyridine-2,6-dicarboxylate (Intermediate D, 1.00 g, 3.81 mmol) in DMF (15 mL) cooled to 0° C. is added 60% sodium hydride in mineral oil (168 mg, 4.19 mmol). The mixture is stirred at 0° C. for 20 min after which a solution of tert-butyl 6-methyl-1,2,3-oxathiazinane-3-carboxylate 2,2-dioxide (1.05 g, 4.19 mmol) in DMF (2 mL) is added. After being stirred overnight, the mixture is concentrated under reduced pressure and the residue is partitioned between ethyl acetate and saturated NaHCO3 solution. The layers are separated and the aqueous layer is further extracted with ethyl acetate. The combined organic phases are washed with brine, and are dried (Na2SO4). The solvent is removed in vacuo and the crude material is purified via flash column chromatography using a gradient elution of 0-30% ethyl acetate/heptanes to afford the title compound as a yellow oil (1.20 g, 73%). LCMS: 434.89 (M+H+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09073926B2
Quelldatensatzuspto-grants-2015_07
ORD IDord-c612bdc7aa7c43efbb62c80b29226a9a
Quellennotizuspto-grants-2015_07