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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16009생성일: 2026년 10월 23일

3,3-Difluoropyrrolidine → (3R)-N-methyl-1-[1-(quinolin-6-ylmethyl)-1H-[1,2,3]triazolo[4,5-b]pyrazin-6-yl]pyrrolidin-3-amine

https://huagongshe.com/ko/reaction/16009

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참여 물질

역할이름HCID투입량
반응물3,3-DifluoropyrrolidineHCID 2782827—
반응물1-[1-(quinolin-6-ylmethyl)-1H-[1,2,3]triazolo[4,5-b]pyrazin-6-yl]pyrrolidin-3-oneHCID 59341815—
용매Tetrahydrofuran methanol dimethylacetamideHCID 86616412—
생성물(3R)-N-methyl-1-[1-(quinolin-6-ylmethyl)-1H-[1,2,3]triazolo[4,5-b]pyrazin-6-yl]pyrrolidin-3-amineHCID 5934185546.2%

반응 조건

온도80 °C

반응 단계

A suspension of 1-[1-(quinolin-6-ylmethyl)-1H-[1,2,3]triazolo[4,5-b]pyrazin-6-yl]pyrrolidin-3-one (50 mg, 0.15 mmol) and 3,3-difluoropyrrolidine (42 mg, 0.29 mmol) in tetrahydrofuran/methanol/dimethylacetamide (1.0 mL each) was heated to 80° C. for 2 hours then NaBCNH3 (18 mg, 0.29 mmol) was added. After 2 hours the solution was cooled to room temperature and concentrated. The crude product was purified by flash chromatography using a Horizon purification system on a 25S column eluting with chloroform/acetone (5-50%) followed by a second column on a 12M cartridge eluting with chloroform/ethyl acetate (25-100%) to afford the title compound (25 mg, 40%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732604B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-5c3e3bb1ce0c4d1096cbf35ede4881e8
출처 메모uspto-grants-2010_06