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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 986745생성일: 2026년 10월 26일

Thiophene, 2-nitro- → Ethyl 7-thienylamino-1H-pyrazolo[4,3-b]pyridine-6-carboxylate

https://huagongshe.com/reaction/986745

반응식

참여 물질

역할이름HCID투입량
반응물Thiophene, 2-nitro-HCID 11866—
반응물2-AminothiopheneHCID 97373—
반응물Ethyl 7-chloro-1H-pyrazolo[4,3-B]pyridine-6-carboxylateHCID 20038759—
촉매PalladiumHCID 23938—
생성물Ethyl 7-thienylamino-1H-pyrazolo[4,3-b]pyridine-6-carboxylateHCID 2015624110.4%

반응 단계

Ethyl 7-chloro-1H-pyrazolo[4,3-b]pyridine-6-carboxylate (4.5 g 0.02 mole) and aminothiophene (2.0 g) [prepared from 2-nitrothiophene (supplied by Aldrich and shown by nmr to contain 15% of 3-nitrothiophene) by reduction using either H2 ; 10% Pd/C or stannous chloride] were stirred together under nitrogen for 24 hours. The ethanol was removed under reduced pressure. The resulting brown oil was purified by column chromatography on silica eluting with 5% methanol/ether to give the title compound as a beige solid (0.600 g), mp 188°-190° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04716160
출처 데이터셋uspto-grants-1987_12
ORD IDord-40304c089c2d43628c76574169abe41e
출처 메모uspto-grants-1987_12