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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 909219생성일: 2026년 10월 27일

N,N-Dimethyl-1,3-propanediamine → N'-[5-(2,4-difluorophenoxy)-1-isobutyl-1H-indazol-6-yl]-N,N-dimethylpropane-1,3-diamine

https://huagongshe.com/reaction/909219

반응식

참여 물질

역할이름HCID투입량
반응물N,N-Dimethyl-1,3-propanediamineHCID 7993—
반응물Binap, (A+-)-HCID 634876—
반응물Sodium t-butoxideHCID 23676156—
반응물6-Bromo-5-(2,4-difluorophenoxy)-1-isobutyl-1H-indazoleHCID 57418762—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매1,4-DioxaneHCID 31275—
생성물N'-[5-(2,4-difluorophenoxy)-1-isobutyl-1H-indazol-6-yl]-N,N-dimethylpropane-1,3-diamineHCID 5763970469.2%

반응 조건

온도100 °C

반응 단계

A mixture of 6-bromo-5-(2,4-difluorophenoxy)-1-isobutyl-1H-indazole (15d; Example 110, Steps A-E) (0.030 g, 0.079 mmol), 3-(dimethylamino)propylamine (0.012 g, 0.118 mmol), BINAP (0.009 g, 0.016 mmol), Pd2 dba3 (0.007 g, 0.008 mmol), and NaOtBu (0.008 g, 0.087 mmol), in dioxane were mixed in a flask and purged with N2 three times. The reaction mixture was then heated to 100° C. for 16 hours. The mixture was cooled to room temperature and partitioned between ethyl acetate (20 mL) and brine (20 mL). The aqueous phase was extracted with ethyl acetate and the combined organics were dried over MgSO4 and concentrated under reduced pressure. The residue was chromatographed on silica eluting with acetone/ether (1:1.5) with 0.2% triethylamine. The product was chromatographed again eluting with 5% MeOH in dichloromethane to afford 0.022 g of the product as colorless oil (69% yield). MS (ESI+) m/z 403 (M+1) detected; 1H NMR (400 mHz, CDCl3) δ 7.70 (s, 1H), 6.95 (m, 3H), 6.80 (m, 1H), 6.40 (s, 1H), 5.48 (br. s, 1H), 4.06 (d, 2H), 3.28 (m, 2H), 2.43 (m, 2H), 2.35 (m, 1H), 2.20 (s, 6H), 1.86 (m, 2H), 0.94 (d, 6H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08017641B2
출처 데이터셋uspto-grants-2011_09
ORD IDord-003d2a904c614145be9a70b7dacdc417
출처 메모uspto-grants-2011_09