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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| 반응물 | 2-Cyclopropyl-4-(trifluoromethyl)benzoic acid | HCID 59438485 | — |
| 반응물 | 4-(Pyrrolidin-1-yl)tetrahydro-2H-pyran-3-amine dihydrochloride | HCID 67360004 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2-Cyclopropyl-N-((3SR,4RS)-4-pyrrolidin-1-yl-tetrahydro-pyran-3-yl)-4-trifluoromethyl-benzamide | HCID 67359255 | 62% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08524909B2 |
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| 출처 데이터셋 | uspto-grants-2013_09 |
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| ORD ID | ord-fac9c8face704ca2b24997f1ae65abf9 |
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| 출처 메모 | uspto-grants-2013_09 |
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