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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133527Generated: October 26, 2026

1-Cyclopropyl-butane-1,3-dione → cyclopropyl-(2-methyl-4-phenyl-6,7-dihydro-5H-cyclopenta[4,5]thieno[2,3-b]pyridin-3-yl)-methanone

https://huagongshe.com/reaction/133527

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Cyclopropyl-butane-1,3-dioneHCID 11018869—
Reactant3-benzoyl-4H,5H,6H-cyclopenta[b]thiophen-2-amineHCID 14241840—
CatalystSulfuric AcidHCID 1118—
SolventAcetic AcidHCID 176—
Productcyclopropyl-(2-methyl-4-phenyl-6,7-dihydro-5H-cyclopenta[4,5]thieno[2,3-b]pyridin-3-yl)-methanoneHCID 1155171733.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a stirred solution of 60 mg (0.24 mmol) (2-amino-5,6-dihydro-4H-cyclopenta[b]thiophen-3-yl)-phenyl-methanone (the preparation of which is described in example 3) in 2 ml acetic acid was added 41 mg (0.32 mmol) of 1-cyclopropyl-butane-1,3-dione (prep. described in the patent DE 94-4404059) 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. Preparative HPLC (30% CH3CN/H20) afforded 27 mg (33%) cyclopropyl-(2-methyl-4-phenyl-6,7-dihydro-5H-cyclopenta[4,5]thieno[2,3-b]pyridin-3-yl)-methanone as a light brown oil. ES-MS m/e (%): 334 (M+H+, 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07390903B2
Source datasetuspto-grants-2008_06
ORD IDord-43d20c40d4484e1397994fb0f40006cf
Source noteuspto-grants-2008_06