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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1422641생성일: 2026년 10월 26일

4H,5H,6H,7H-thieno(2,3-c)pyridine → {(S)-6-[(R)-4-(4,7-Dihydro-thieno[2,3-c]pyridin-6-ylmethyl)-5-trifluoromethyl-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid

https://huagongshe.com/reaction/1422641

반응식

참여 물질

역할이름HCID투입량
반응물4H,5H,6H,7H-thieno(2,3-c)pyridineHCID 12337025—
반응물{(S)-6-[(R)-4-Bromomethyl-5-trifluoromethyl-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl esterHCID 86700813—
반응물HCID 90314437HCID 90314437—
생성물{(S)-6-[(R)-4-(4,7-Dihydro-thieno[2,3-c]pyridin-6-ylmethyl)-5-trifluoromethyl-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acidHCID 90313752—

반응 단계

The methyl ester of the title compound, {(S)-6-[(R)-4-(4,7-dihydro-thieno[2,3-c]pyridin-6-ylmethyl)-5-trifluoromethyl-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl ester, is prepared from {(S)-6-[(R)-4-bromomethyl-5-trifluoromethyl-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl ester and 4,5,6,7-tetrahydro-thieno[2,3-c]pyridine following a procedure analogous to that described for Intermediate 42. The crude product is directly submitted to the saponification conditions described for Example 1 to give the title compound upon chromatography on reversed phase (HPLC; acetonitrile/water). LC (method 6): tR=0.91 min; Mass spectrum (ESI+): m/z=530 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08927531B2
출처 데이터셋uspto-grants-2015_01
ORD IDord-fa9637142d1e408089f14bc1e7e14d71
출처 메모uspto-grants-2015_01