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HRID 581206생성일: 2026년 10월 25일

Cesium carbonate → 4-Methoxybenzyl 2-[(3S,4S)-4-t-Butyldimethylsilyloxymethyl-2-oxo-3-tritylaminoazetidin-1-yl]acetate

https://huagongshe.com/reaction/581206

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물4-Methoxybenzyl 2-bromoacetateHCID 13233234—
반응물(3S,4S)-4-t-Butyldimethylsilyloxymethyl-3-tritylaminoazetidinoneHCID 13859068—
용매DimethylformamideHCID 6228—
용매AcetonitrileHCID 6342—
생성물4-Methoxybenzyl 2-[(3S,4S)-4-t-Butyldimethylsilyloxymethyl-2-oxo-3-tritylaminoazetidin-1-yl]acetateHCID 70200031114.7%

반응 단계

Cesium carbonate (1.58 g) was added to a stirred solution of (3S,4S)-4-t-butyldimethylsilyloxymethyl-3-tritylaminoazetidin-2-one (1.45 g) (IV) (H. Mastalerz et al., J. Med. Chem., 1988, 31, 1190-1196) in a mixture of acetonitrile (44 ml) and dimethylformamide (35 ml). 4-Methoxybenzyl bromoacetate (1.44 g) was then added and the mixture stirred at room temperature for 48 h. The mixture was then partitioned between ethyl acetate and water, the organic phase was washed four times with water, and then with brine. The solution was dried over magnesium sulphate and evaporated. The title compound (2.29 g) was isolated by column chromatography of the residue (Silica gel, 3:1 hexane:ethyl acetate as eluent). [α]D21 -9.0°; νmax (CHCl3) 3352, and 1755 cm-1 ; δ(CDCl3) -0.04 (3H, s), 0.00 (3H, s), 0.88 (9H, s), 1.69 (1H, br s), 2.54 (1H, dd, J 3.33 and 11.68 Hz), 3.19 (1H, dd, J 2.05 and 11.68 Hz), 3.38 (1H, m), 3.51 (1H, d, J 17.98 Hz), 3.90 (3H, s), 4.46 (1H, d, J 17.98 Hz), 4.54 (1H, m), 5.06 (1H, d, J 11.79 Hz), 5.15 (1H, d, J 11.81 Hz), 6.94 (2H, d, J 8.68 Hz), 7.2-7.65 (17H, m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05919925
출처 데이터셋uspto-grants-1999_07
ORD IDord-62ab2a671d1041e3a046ded22a219a9b
출처 메모uspto-grants-1999_07