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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1047685생성일: 2026년 10월 26일

2-Bromopropane → 4-(2-Isopropoxy-3-methyl-benzoylamino)-tetrahydro-thiopyran-4-carboxylic acid methyl ester

https://huagongshe.com/reaction/1047685

반응식

참여 물질

역할이름HCID투입량
반응물2-BromopropaneHCID 6358—
반응물Cesium carbonateHCID 10796—
반응물4-(2-Hydroxy-3-methyl-benzoylamino)-tetrahydro-thiopyran-4-carboxylic acid methyl esterHCID 59314262—
용매DimethylformamideHCID 6228—
생성물4-(2-Isopropoxy-3-methyl-benzoylamino)-tetrahydro-thiopyran-4-carboxylic acid methyl esterHCID 5931418981.8%

반응 단계

To a suspension of 4-(2-hydroxy-3-methyl-benzoylamino)-tetrahydro-thiopyran-4-carboxylic acid methyl ester (27) (98 mg, 0.32 mmol), anhydrous Cs2CO3 (208 mg, 0.64 mmol), and KI (11 mg, 0.06 mmol) in DMF (5 mL) is added 2-bromopropane (150 μL, 1.6 mmol). The resulting reaction suspension is stirred at RT overnight. After the removal of DMF in vacuo, the residue is dissolved in EtOAc (20 mL) and washed with water (1×5 mL) and brine (2×5 mL). The organic layer is dried over anhydrous Na2SO4 and concentrated in vacuo. The residue is purified by flash column chromatography (80 g silica gel, gradient elution: 5-40% EtOAc in heptane) to give a pure product (28) as white solid (92 mg, 81%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08569535B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-dc112b9fcc0246cba4432651c7307afc
출처 메모uspto-grants-2013_10