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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1643500생성일: 2026년 10월 26일

Dimethyl Sulfoxide → Biphenyl-2-ylcarbamic Acid 1-[2-(3-formylbenzylcarbamoyl)ethyl]piperidin-4-yl Ester

https://huagongshe.com/reaction/1643500

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물DiisopropylethylamineHCID 81531—
반응물Sulfur trioxide-pyridineHCID 168533—
반응물Biphenyl-2-ylcarbamic acid 1-[2-(3-hydroxymethylbenzylcarbamoyl)ethyl]piperidin-4-yl EsterHCID 59340333—
용매DichloromethaneHCID 6344—
생성물Biphenyl-2-ylcarbamic Acid 1-[2-(3-formylbenzylcarbamoyl)ethyl]piperidin-4-yl EsterHCID 59340336—

반응 조건

온도-10 °C

반응 단계

To a flask was added biphenyl-2-ylcarbamic acid 1-[2-(3-hydroxymethylbenzyl carbamoyl)ethyl]piperidin-4-yl ester (0.33 g, 0.68 mmol; prepared as described in Preparation 12), DCM (5 mL), DIPEA (0.47 mL, 2.7 mol) and DMSO (0.2 mL, 2.7 mol). Using an ice bath, the mixture was cooled to about −10° C. and sulfur trioxide pyridine-complex (0.32 g, 2.0 mol) was added. The reaction was stirred at −10° C. for 0.75 hour. Before removing the ice-bath, the reaction was quenched by adding water (5 mL). The aqueous layer was separated and the organic layer was washed with water (2×5 mL), 1.0N NaHSO4(aq) (2×5 mL), 1.0N NaHCO3(aq) (1×5 mL) and brine (0.5 L) and then dried over MgSO4 and filtered to provide the title compound which was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08119796B2
출처 데이터셋uspto-grants-2012_02
ORD IDord-bc16a827c36c4d2787d08a014512d8a1
출처 메모uspto-grants-2012_02