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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2234492생성일: 2026년 10월 26일

4-Amino-3-fluorobenzoic acid → 4-amino-N-(1-ethylpiperidin-4-yl)-3-fluorobenzamide

https://huagongshe.com/reaction/2234492

반응식

참여 물질

역할이름HCID투입량
반응물4-Amino-3-fluorobenzoic acidHCID 9971—
반응물DiisopropylethylamineHCID 81531—
반응물1-Ethylpiperidin-4-amineHCID 3734990—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
용매DimethylacetamideHCID 31374—
생성물4-amino-N-(1-ethylpiperidin-4-yl)-3-fluorobenzamideHCID 5510278222.7%

반응 단계

4-amino-3-fluorobenzoic acid (2.115 g, 13.6 mmol), 4-Amino-1-Ethyl Piperidine (Fluorochem; 1.923 g, 15 mmol), HATU (5.7 g, 15 mmol) and DIPEA (7.1 mL, 40.8 mmol) were combined in DMA (60 mL) and the resulting yellow solution stirred at room temperature for 20 minutes. The reaction was left over the weekend at room temperature, solvent evaporated and the residue dissolved in methanol (10 mL) and loaded onto an SCX-2 column (50 g) which pre-wet with MeOH (40 mL), flushed with MeOH (4×30 ml) and eluted with 7N ammonia in MeOH (4×30 mL). Product containing, ammoniacal fractions were combined to yield the title compound as a brown solid (0.819 g, 22%)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07709471B2
출처 데이터셋uspto-grants-2010_05
ORD IDord-60cb88dc051744b899d25578ed6a4372
출처 메모uspto-grants-2010_05