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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 926872생성일: 2026년 10월 24일

Diisopropylethylamine → HCID 66587597, 화합물

https://huagongshe.com/ko/reaction/926872

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—
반응물1H-Pyrazol-3-amine, 1-[3-(trifluoromethyl)phenyl]-HCID 13626946—
반응물2-Nitro-5-(piperidin-1-yl)benzoic acidHCID 14459331—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물HCID 66587597HCID 6658759736.4%

반응 조건

온도50 °C

반응 단계

Into a 250-mL round bottom flask, was placed a solution of 2-nitro-5-(piperidin-1-yl)benzoic acid (5 g, 20.00 mmol, 1.19 equiv) in N,N-dimethylformamide (50 mL), 1-(3-(trifluoromethyl)phenyl)-1H-pyrazol-3-amine (3.8 g, 16.74 mmol, 1.00 equiv), HATU (9.5 g, 25.00 mmol, 1.49 equiv), and N,N-diisopropylethylamine (3.3 g, 25.58 mmol, 1.53 equiv). The resulting solution was stirred overnight at 50° C. in an oil bath. The reaction progress was monitored by LCMS. The resulting solution was diluted with 200 mL of water, extracted with 4×50 mL of ethyl acetate, and the organic layers combined. The resulting mixture was washed with 2×50 mL of water and 2×50 mL of brine. The mixture was dried over sodium sulfate. The solids were filtered out. The resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column and eluted with petroleum ether/ethyl acetate (5:1) to yield 2.8 g (36%) of product as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09289430B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-15e29229d098487dbe70c98bd9b953b5
출처 메모uspto-grants-2016_03