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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 133529생성일: 2026년 10월 26일

(2-Amino-5,6-dihydro-4H-cyclopenta[b]thiophen-3-yl)-thiophen-2-yl-methanone → cyclopropyl-(2-methyl-4-thiophen-2-yl-6,7-dihydro-5H-cyclopenta[4.5]thieno[2,3-b]pyridin-3-yl)-methanone

https://huagongshe.com/reaction/133529

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참여 물질

역할이름HCID투입량
반응물(2-Amino-5,6-dihydro-4H-cyclopenta[b]thiophen-3-yl)-thiophen-2-yl-methanoneHCID 9899694—
반응물1-Cyclopropyl-butane-1,3-dioneHCID 11018869—
촉매Sulfuric AcidHCID 1118—
용매Acetic AcidHCID 176—
생성물cyclopropyl-(2-methyl-4-thiophen-2-yl-6,7-dihydro-5H-cyclopenta[4.5]thieno[2,3-b]pyridin-3-yl)-methanoneHCID 1170284819%

반응 조건

온도100 °C

반응 단계

To a stirred solution of 60 mg (0.24 mmol) (2-amino-5,6-dihydro-4H-cyclopenta[b]thiophen-3-yl)-thiophen-2-yl-methanone) (the preparation of which is described in example 2) in 2 ml acetic acid was added 40 mg (0.32 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. Preparative HPLC (30% CH3CN/H20) afforded 15 mg (19%) cyclopropyl-(2-methyl-4-thiophen-2-yl-6,7-dihydro-5H-cyclopenta[4.5]thieno[2,3-b]pyridin-3-yl)-methanone as a light brown oil. ES-MS m/e (%): 340 (M+H+, 100).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07390903B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-d2dc0072d49e451f839ba50dedf64c0d
출처 메모uspto-grants-2008_06