Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Thiophene, 2-nitro- → Ethyl 7-thienylamino-1H-pyrazolo[4,3-b]pyridine-6-carboxylate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Thiophene, 2-nitro- | HCID 11866 | — |
| 반응물 | 2-Aminothiophene | HCID 97373 | — |
| 반응물 | Ethyl 7-chloro-1H-pyrazolo[4,3-B]pyridine-6-carboxylate | HCID 20038759 | — |
| 촉매 | Palladium | HCID 23938 | — |
| 생성물 | Ethyl 7-thienylamino-1H-pyrazolo[4,3-b]pyridine-6-carboxylate | HCID 20156241 | 10.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04716160 |
| 출처 데이터셋 | uspto-grants-1987_12 |
| ORD ID | ord-40304c089c2d43628c76574169abe41e |
| 출처 메모 | uspto-grants-1987_12 |