돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 39437생성일: 2026년 10월 24일

Diisopropylethylamine → 2-Cyclopropyl-N-((3SR,4RS)-4-pyrrolidin-1-yl-tetrahydro-pyran-3-yl)-4-trifluoromethyl-benzamide

https://huagongshe.com/ko/reaction/39437

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물2-Cyclopropyl-4-(trifluoromethyl)benzoic acidHCID 59438485—
반응물4-(Pyrrolidin-1-yl)tetrahydro-2H-pyran-3-amine dihydrochlorideHCID 67360004—
용매DimethylformamideHCID 6228—
생성물2-Cyclopropyl-N-((3SR,4RS)-4-pyrrolidin-1-yl-tetrahydro-pyran-3-yl)-4-trifluoromethyl-benzamideHCID 6735925562%

반응 단계

2-Cyclopropyl-4-trifluoromethyl-benzoic acid (intermediate J, 118 mg, 0.513 mmol) was dissolved in 2.5 mL dimethylformamide. N,N-Diisopropyl ethyl amine (338 mg, 2.62 mmol) and O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (195 mg, 0.513 mmol) were added. After 10 minutes of stirring at room temperature trans-(4-pyrrolidin-1-yl-tetrahydro-pyran-3-ylamine dihydrochloride (intermediate 1,187 mg, 0.769 mmol) was added. The reaction mixture was stirred at room temperature overnight. The solvent was evaporated off. The residue was taken up in 2N sodium carbonate solution and ethyl acetate and was extracted three times with ethyl acetate. The combined organic phases were dried on sodium sulfate, filtered and evaporated. Purification of the residue by flash chromatography on silica gel (heptane/ethyl acetate/triethylamine 1:0:0→10:10:1) yielded the title compound as a white solid (121 mg, 62%), MS: m/e=383.3 [(M+H)+].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524909B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-fac9c8face704ca2b24997f1ae65abf9
출처 메모uspto-grants-2013_09