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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 220330생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/220330

반응식

참여 물질

역할이름HCID투입량
반응물Oxalyl chlorideHCID 65578—
반응물2-Thiopheneglyoxylic acidHCID 77694—
반응물DiisopropylethylamineHCID 81531—
반응물N,N-Dimethylpiperidin-4-amineHCID 417391—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물1-(4-Dimethylaminopiperidin-1-yl)-2-thiophen-2-yl-ethane-1,2-dioneHCID 5982852398.4%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08202891B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-41b1e7b8df8c44c797c03d084b8e46d5
출처 메모uspto-grants-2012_06