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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1792531생성일: 2026년 10월 26일

Tributyltin Chloride → 5-{6-[3-(4-Fluorophenyl)-1-trityl-1H-4-pyrazolyl]imidazo-[1,2-a]pyridin-3-yl}-2-thiophene carboxamide

https://huagongshe.com/reaction/1792531

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참여 물질

역할이름HCID투입량
반응물Tributyltin ChlorideHCID 15096—
반응물5-Bromothiophene-2-carboxamideHCID 605722—
반응물6-[3-(4-fluorophenyl)-1-trityl-1H-pyrazolyl]-3-iodoimidazo[1,2-a]pyridineHCID 22031070—
용매O-XyleneHCID 7237—
생성물5-{6-[3-(4-Fluorophenyl)-1-trityl-1H-4-pyrazolyl]imidazo-[1,2-a]pyridin-3-yl}-2-thiophene carboxamideHCID 22031978—

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온도120 °C

반응 단계

A mixture of 200 mg 6-[3-(4-fluorophenyl)-1-trityl-1H-4-pyrazolyl]-3-(1,1,1-tributylstannyl)imidazo[1,2-a]-pyridine prepared from 6-[3-(4-fluorophenyl)-1-trityl-1H-4-pyrazolyl]-3-iodoimidazo[1,2-a]pyridine (compound in Production Example 39) and tributyltin chloride by the same method as in Production Example 48, 51 mg 5-bromo-2-thiophene carboxamide, 14 mg tetrakis (triphenylphosphine)palladium and 3 mL xylene was stirred at 120° C. for 2 hours under nitrogen atmosphere. The solvent was evaporated, and the residue was purified by silica gel chromatography (ethyl acetate/methanol) to give 37 mg of the title compound as a colorless amorphous.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07074801B1
출처 데이터셋uspto-grants-2006_07
ORD IDord-896734599f244f34b0c84bd5a29ad4fd
출처 메모uspto-grants-2006_07