戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 220330作成日:2026年10月26日

Oxalyl chloride → 1-(4-Dimethylaminopiperidin-1-yl)-2-thiophen-2-yl-ethane-1,2-dione

https://huagongshe.com/reaction/220330

反応式

関与物質

役割名称HCID仕込み量
反応物Oxalyl chlorideHCID 65578—
反応物2-Thiopheneglyoxylic acidHCID 77694—
反応物DiisopropylethylamineHCID 81531—
反応物N,N-Dimethylpiperidin-4-amineHCID 417391—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物1-(4-Dimethylaminopiperidin-1-yl)-2-thiophen-2-yl-ethane-1,2-dioneHCID 5982852398.4%

反応手順

2-Thiopheneglyoxylic acid (300 mg, 1.9 mmol) was dissolved in 10 mL of methylene chloride. A 2.0 M solution of oxalyl chloride in methylene chloride (1.1 mL, 2.1 mmol) was then added, followed by 10 μL of DMF. The resulting solution was stirred at room temperature for 1 hour, then a solution of dimethylpiperidin-4-ylamine (271 mg, 2.1 mmol) and DIPEA (1.0 mL, 5.8 mmol) in 2 mL of methylene chloride was added. 4-Dimethylaminopyridine (12 mg, 96 μmol) was then added and the resulting mixture was stirred at room temperature for 2 hours. The mixture was then extracted with a saturated sodium bicarbonate solution, and the organic layer was dried over Na2SO4 and concentrated to yield the crude intermediate (4a) (498 mg), which was used in the next step without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08202891B2
出典データセットuspto-grants-2012_06
ORD IDord-41b1e7b8df8c44c797c03d084b8e46d5
出典メモuspto-grants-2012_06