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HRID 2389269作成日:2026年10月27日

Triethylamine → Tert-butyl 4-(2-cyano-1-benzofuran-5-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2389269

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Trifluoroacetic anhydrideHCID 9845—
反応物Tert-butyl 4-(2-carbamoylbenzofuran-5-yl)piperazine-1-carboxylateHCID 11244883—
溶媒DichloromethaneHCID 6344—
生成物Tert-butyl 4-(2-cyano-1-benzofuran-5-yl)piperazine-1-carboxylateHCID 67154775—

反応条件

温度0 °C

反応手順

The tert-butyl 4-[2-(aminocarbonyl)-1-benzofuran-5-yl]piperazine-1-carboxylate (85 mg, 0.246 mmol) was dissolved in 5 mL of DCM and cooled to 0° C. under nitrogen. Triethylamine (0.075 mL, 0.541 mmol) was added, followed by trifluoroacetic anhydride (0.038 mL, 0.271 mmol). The reaction was stirred for 1 hour, then was diluted with additional 20 mL of DCM and washed with water (2×40 mL). The organic layers were combined, dried over sodium sulfate, filtered and concentrated to afford tert-butyl 4-(2-cyano-1-benzofuran-5-yl)piperazine-1-carboxylate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08273737B2
出典データセットuspto-grants-2012_09
ORD IDord-e1c2fb2a86d248208d1585cf22ab9967
出典メモuspto-grants-2012_09