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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1072983Erstellt: 26. Oktober 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → Methyl furo[3,2-c]pyridine-6-carboxylate

https://huagongshe.com/reaction/1072983

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
EduktMethyl 2-acetamido-2-(dimethoxyphosphoryl)acetateHCID 11746707—
EduktFuran-2,3-dicarbaldehydeHCID 13814199—
LösungsmittelChloroformHCID 6212—
ProduktMethyl furo[3,2-c]pyridine-6-carboxylateHCID 2204728082,5%

Reaktionsschritte

Methyl (acetylamino)(dimethoxyphosphoryl)acetate (2.34 g, 9.8 mmol) is dissolved in CHCl3 (40 mL), treated with DBU (1.46 mL, 9.8 mmol), stirred for 5 min then added dropwise to a 0° C. solution of furan-2,3-dicarbaldehyde (1.65 g, 8.9 mmol) in CHCl3 (80 mL). The mixture is stirred for 2.5 h as the cooling bath expires then 5.5 h at RT and finally 24 h at 50° C. The mixture is concentrated in vacuo to a yellow oily-solid (6.66 g). The crude material is chromatographed over a standard 100 g slurry-packed silica gel, eluting with 65% EtOAc/hexane. The appropriate fractions are combined and concentrated in vacuo to afford 1.30 g (82%) of methyl furo[3,2-c]pyridine-6-carboxylate as a yellow solid. MS (EI) m/z: 177 (M+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06911543B2
Quelldatensatzuspto-grants-2005_06
ORD IDord-fcefbc1462f44d78a8a1d9d47c30686d
Quellennotizuspto-grants-2005_06