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HRID 55816作成日:2026年10月24日

Triethylamine → Methyl 1-(6-methoxy-3-(trifluoromethyl)quinolin-2-yl)piperidine-4-carboxylate

https://huagongshe.com/ja/reaction/55816

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Methyl isonipecotateHCID 424914—
反応物2-Chloro-6-methoxy-3-(trifluoromethyl)quinolineHCID 86689936—
溶媒WaterHCID 962—
溶媒IsopropanolHCID 3776—
生成物Methyl 1-(6-methoxy-3-(trifluoromethyl)quinolin-2-yl)piperidine-4-carboxylateHCID 6698010843%

反応手順

To a solution of 2-chloro-6-methoxy-3-(trifluoromethyl)quinoline (1.00 g, 3.85 mmol) (see Intermediate 6, Step 8 for synthesis) in IPA (5 mL) was added methyl-4-piperidinecarboxylate (5.50 g, 38.5 mmol) and Et3N (1.17 g, 11.6 mmol). The mixture was heated to reflux for 48 hours. The mixture was diluted with water (100 mL) and extracted with DCM (100 mL×3), the combined organic layers were washed with brine (200 mL), dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure to give the crude product, which was purified by column chromatography on silica gel (PE/EtOAc=15/1) to give the product (600 mg, yield 43%) as a solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09433618B2
出典データセットuspto-grants-2016_09
ORD IDord-91f426121a724ce7aa13b19804805233
出典メモuspto-grants-2016_09