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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2196699Erstellt: 25. Oktober 2026

1-(Phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine-3-carbaldehyde → 1H-Pyrrolo[2,3-b]pyridine-3-methanol, a-cyclopropyl-1-(phenylsulfonyl)-

https://huagongshe.com/reaction/2196699

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-(Phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine-3-carbaldehydeHCID 10356646—
EduktHCID 178478986HCID 178478986—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1H-Pyrrolo[2,3-b]pyridine-3-methanol, a-cyclopropyl-1-(phenylsulfonyl)-HCID 6715576498%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

1-(Phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine-3-carbaldehyde (0.25 g, 0.87 mmol) was dissolved in dry THF (9 mL) and chilled to 0° C. Cyclopropylmagnesium chloride (2.6 mL of a 0.5M solution in THF, 1.5 eq.) was then added by syringe to the cold reaction mixture and stirred at 0° C. for 30 minutes. The mixture was then quenched with saturated ammonium chloride solution, extracted with EtOAc, extracts dried over sodium sulfate and concentrated to provide cyclopropyl(1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-3-yl)methanol (0.285 g, 98%). m/z (APCI-pos) M+1=329.1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08338452B2
Quelldatensatzuspto-grants-2012_12
ORD IDord-29bab400bff446939511ad3f27f84817
Quellennotizuspto-grants-2012_12