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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 857455Erstellt: 25. Oktober 2026

Methyl chloroformate → Ethyl 6-chloro-1H-pyrrolo[2,3-b]pyridine-2-carboxylate

https://huagongshe.com/reaction/857455

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl chloroformateHCID 6586—
EduktHCID 178468513HCID 178468513—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktEthyl 6-chloro-1H-pyrrolo[2,3-b]pyridine-2-carboxylateHCID 2186875826,4%

Reaktionsschritte

To a stirred solution of ethyl 7-azaindole-2-carboxylate-7-oxide (1.32 g, 6.4 mmol) and hexamethyldisilazale (1.4 mL, 6.6 mmol) in THF (30 mL) at 0° C. was added dropwise over 30 min a solution of methyl chloroformate (1.2 mL, 15.5 mmol) in THF (5 mL). The mixture was warmed to room temperature, stirred for 2 h and partitioned between ether (50 mL) and water (50 mL). The aqueous layer was extracted with ether (30 mL). The combined organic extracts were washed (water, brine), dried (sodium sulfate) and purified by column chromatography [SiO2; heptane-ether (3:1)] to give ethyl 6-chloro-7-azaindole-2-carboxylate as a white solid (0.38 g, 26%). mp 144–145° C. Found: C, 53.69; H, 4.05; N, 12.39%. C10H9N2ClO2 requires: C, 53.47; H, 4.04; N, 12.46%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07145009B2
Quelldatensatzuspto-grants-2006_12
ORD IDord-22f1a90dea4d4b10a3dbc241cfc90e39
Quellennotizuspto-grants-2006_12