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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 220332생성일: 2026년 10월 25일

Dichloromethane → 1-(4-Dimethylamino-piperidin-1-yl)-2-hydroxy-2,2-di-thiophen-2-ylethanone

https://huagongshe.com/reaction/220332

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물TetrahydrofuranHCID 8028—
반응물Oxalyl chlorideHCID 65578—
반응물2-Thiopheneglyoxylic acidHCID 77694—
반응물DiisopropylethylamineHCID 81531—
반응물N,N-Dimethylpiperidin-4-amineHCID 417391—
반응물HCID 178418438HCID 178418438—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DimethylformamideHCID 6228—
생성물1-(4-Dimethylamino-piperidin-1-yl)-2-hydroxy-2,2-di-thiophen-2-ylethanoneHCID 59828527—

반응 조건

온도0 °C

반응 단계

To a stirred solution of 2-thiopheneglyoxylic acid (1.0 g, 6.4 mmol) in DCM (100 mL, 2 mol), was added oxalyl chloride (596 μL, 7 mmol) and a catalytic amount of DMF. The mixture was stirred for 2 hours and then was cooled at 0° C. in an ice bath. Dimethyl-piperidin-4-ylamine (821 mg, 6.4 mmol), DIPEA (1.7 mL, 9.6 mmol) and DMAP (20 mg, 0.1 mmol) were added, and the mixture was stirred for 2 hours. The solvent was removed under reduced pressure and the crude mixture was then dissolved in DCM (60 mL), washed with a saturated bicarbonate solution (50 mL), and dried over MgSO4. The solvent was removed under reduced pressure and the crude material was then dissolved in THF (50 mL, 0.6 mol) and cooled to 0° C. in an ice bath. To the stirred solution was added 1.0 M thiophen-2-yl magnesium bromide in THF (7.7 mL, 7.7 mmol) was added. The mixture was stirred for 30 minutes, then quenched with a saturated bicarbonate solution (50 mL) and DCM (50 mL). The organic was taken and dried over MgSO4, and the solvent was removed under reduced pressure, to afford the title compound (1.5 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08202891B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-61b81f85042e4cc6a30b78aa8ac3033d
출처 메모uspto-grants-2012_06