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HRID 2409849作成日:2026年10月25日

Diisopropylethylamine → HCID 66587597、化合物

https://huagongshe.com/reaction/2409849

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
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—
反応物1-(3-(trifluoromethyl)phenyl)-1H-pyrazol-3-amineHCID 13626946—
反応物2-Nitro-5-(piperidin-1-yl)benzoic acidHCID 14459331—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物HCID 66587597HCID 6658759736.4%

反応条件

温度50 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08815910B2
出典データセットuspto-grants-2014_08
ORD IDord-20c436a577664e0598bd6cb2c89fffdf
出典メモuspto-grants-2014_08