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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1012689생성일: 2026년 10월 26일

Diisopropylethylamine → N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-6-bromo-1-benzofuran-2-carboxamide

https://huagongshe.com/reaction/1012689

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물6-Bromo-1-benzofuran-2-carboxylic acidHCID 1474471—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물(R)-(+)-3-Aminoquinuclidine DihydrochlorideHCID 12494972—
용매MethanolHCID 887—
용매DimethylformamideHCID 6228—
생성물N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-6-bromo-1-benzofuran-2-carboxamideHCID 59341401—

반응 단계

3.8 g (15.77 mmol) of 6-bromobenzofuran-2-carboxylic acid (Example 1A), 3.14 g (15.77 mmol) of (R)-3-aminoquinuclidine dihydrochloride, 7.19 g (18.92 mmol) of HATU, 7.34 g (56.76 mmol) of N,N-diisopropylethylamine and 50 ml of DMF are reacted by general method C. The crude product is taken up in methanol and shaken together with acidic ion exchanger (Dowex® WX2-200) for about 20 min. The loaded ion exchanger is washed successively with methanol, dichloromethane and again with methanol. The product is eluted with methanol/triethylamine 90:10. The solvent is removed in a rotary evaporator under reduced pressure. Finally, the last residues of solvent are removed under high vacuum. 5.14 g (85% of theory) of the title compound are isolated. For analysis, a small amount is converted into the hydrochloride with 4 N hydrogen chloride in dioxane.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07977485B2
출처 데이터셋uspto-grants-2011_07
ORD IDord-ca97488e0c5b48c48236783b99b4c72e
출처 메모uspto-grants-2011_07