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HRID 2234492作成日:2026年10月27日

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

https://huagongshe.com/reaction/2234492

反応式

関与物質

役割名称HCID仕込み量
反応物4-Amino-3-fluorobenzoic acidHCID 9971—
反応物DiisopropylethylamineHCID 81531—
反応物1-Ethylpiperidin-4-amineHCID 3734990—
反応物Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
溶媒DimethylacetamideHCID 31374—
生成物4-amino-N-(1-ethylpiperidin-4-yl)-3-fluorobenzamideHCID 5510278222.7%

反応手順

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%)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07709471B2
出典データセットuspto-grants-2010_05
ORD IDord-60cb88dc051744b899d25578ed6a4372
出典メモuspto-grants-2010_05