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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 133528Erstellt: 24. Oktober 2026

(2-Aminothiophen-3-yl)(phenyl)methanone → Cyclopropyl-(6-methyl-4-phenyl-thieno[2,3-b]pyridin-5-yl)-methanone

https://huagongshe.com/de/reaction/133528

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(2-Aminothiophen-3-yl)(phenyl)methanoneHCID 644720—
Edukt1-Cyclopropyl-butane-1,3-dioneHCID 11018869—
KatalysatorSulfuric AcidHCID 1118—
LösungsmittelAcetic AcidHCID 176—
ProduktCyclopropyl-(6-methyl-4-phenyl-thieno[2,3-b]pyridin-5-yl)-methanoneHCID 115148438,2%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a stirred solution of 60 mg (0.29 mmol) (2-amino-thiophen-3-yl)-phenyl-methanone (the preparation of which is described in example 20) in 2 ml acetic acid was added 50 mg (0.39 mmol) of 1-cyclopropyl-butane-1,3-dione and one drop of sulfuric acid. The mixture was then stirred at 100° C. for 10 minutes in a microwave and then concentrated in vacuo. Flash chromatography (heptane/ethyl acetate 6:1) afforded 7 mg (8%) cyclopropyl-(6-methyl-4-phenyl-thieno[2,3-b]pyridin-5-yl)-methanone as a colorless oil. ES-MS m/e (%): 294 (M+H+, 100).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07390903B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-7f8697feb0854967a8b7977ce8ccc7c8
Quellennotizuspto-grants-2008_06