Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 69270생성일: 2026년 10월 25일
Potassium Fluoride → (Rac)-{1-[3-(7-fluoro-quinolin-6-ylmethyl)-imidazo[1,2-b]pyridazin-6-yl]-pyrrolidin-3-yl}-methyl-carbamic acid tert-butyl ester
https://huagongshe.com/reaction/69270
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Potassium Fluoride | HCID 522689 | — |
| 반응물 | 3-(N-tert-Butoxycarbonyl-N-methylamino)pyrrolidine | HCID 2761404 | — |
| 반응물 | 6-(6-Chloro-imidazo[1,2-b]pyridazin-3-ylmethyl)-7-fluoro-quinoline | HCID 58147516 | — |
| 용매 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 용매 | tert-Butyl methyl ether | HCID 15413 | — |
| 생성물 | (Rac)-{1-[3-(7-fluoro-quinolin-6-ylmethyl)-imidazo[1,2-b]pyridazin-6-yl]-pyrrolidin-3-yl}-methyl-carbamic acid tert-butyl ester | HCID 68630829 | — |
반응 단계
6-(6-Chloro-imidazo[1,2-b]pyridazin-3-ylmethyl)-7-fluoro-quinoline (Stage 173.1, 150 mg, 0.474 mmol), KF (139 mg, 2.372 mmol) and (rac)-methyl-pyrrolidin-3-yl-carbamic acid tert-butyl ester (285 mg, 1.423 mmol) were suspended in NMP (1.5 mL). The RM was stirred at 170° C. for 1 h. The mixture was diluted with TBME and washed with water (3×). The aqueous phases were further extracted with TBME (1×). The combined organic layer was dried over Na2SO4, filtered and concentrated in vacuo. The residue was crystallized in Et2O to afford the title compound as a beige solid (tR 3.91 min (conditions 13), MH+=477).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08822468B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-69c857447bb649fdbad863c547a7bccb |
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| 출처 메모 | uspto-grants-2014_09 |
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