Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 460352생성일: 2026년 10월 24일
Diisopropylethylamine → 1-[3-(3-Fluoro-phenylamino)-6,7-dimethoxy-4H-indeno[1,2-c]pyrazol-1-yl]-2-hydroxy-ethanone
https://huagongshe.com/ko/reaction/460352
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | Benzyloxyacetyl chloride | HCID 177085 | — |
| 반응물 | Jnj-10198409 | HCID 9797370 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 1-[3-(3-Fluoro-phenylamino)-6,7-dimethoxy-4H-indeno[1,2-c]pyrazol-1-yl]-2-hydroxy-ethanone | HCID 18445440 | 90% |
반응 단계
To a mixture of (6,7-Dimethoxy-1,4-dihydro-indeno[1,2-c]pyrazol-3-yl)-(3-fluoro-phenyl)-amine (Compound 14) (3.6 g, 10.0 mmol), Benzyloxy-acetyl chloride (Compound 27a) (2.2 g, 12.0 mmole) and DMF (50 mL) was added Diisopropylethylamine (5.2 mL, 30 mmole) at room temperature with stirring. The reaction was stirred at room temperature over night. The reaction was quenched with water and extracted with EtOAc. Dried over sodium sulfate and removed solvent in vacuo. The crude material was then taken up into ethanol and 0.5 g of Pd/C was added. The reaction was shaken on the hydrogenator over night. The reaction was filtered through Celite and removed solvent in vacuo. Triturated in a small amount of EtOAc. 3.2 g of ˜90% pure material was produced. 300 mg of the crude material was prepped on the Gilson and lyophilization gave Compound 432 as a white powder. MS m/z 384 (M+H)+;
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07196110B2 |
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| 출처 데이터셋 | uspto-grants-2007_03 |
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| ORD ID | ord-149543929f314c7a99415f9992e517d4 |
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| 출처 메모 | uspto-grants-2007_03 |
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