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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 968520생성일: 2026년 10월 25일

Dicyclohexylcarbodiimide → 2-{[(3r)-4-(4-Toluenesulfonyl)thiomorpholine-3-carbonyl]amino}-3-methyl-butyric acid benzyl ester

https://huagongshe.com/reaction/968520

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물O-benzyl-L-valine toluene-p-sulphonateHCID 11567066—
반응물(3R)-4-(4-toluenesulfonyl)thiomorpholine-3-carboxylic acidHCID 69415969—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물2-{[(3r)-4-(4-Toluenesulfonyl)thiomorpholine-3-carbonyl]amino}-3-methyl-butyric acid benzyl esterHCID 6941607940.8%

반응 단계

0.301 g (1 mmol) of (3R)-4-(4-toluenesulfonyl)thiomorpholine-3-carboxylic acid, 0.417 g (1.1 mmol) of L-valine benzyl ester p-toluenesulfonic acid salt, 0.227 g (1.2 mmol) of DCC and 0.122 g (1 mmol) of DMAP were dissolved in 30 mL of CH2Cl2, 0.2 ml (1.4 mmol) of TEA was added. The mixture was stirred for 24 h at room temperature. The solid was filtrated and the solvent was evaporated. The residual was dissolved in a suitable amount of ethyl acetate (20 ml) and then the mixture was filtered to remove insoluble substance. The ethyl acetate was added to 60 ml and then the liquid was washed with 10% NaHCO3 solution, saturated NaCl solution and dried over Na2SO4. After the drying agent was removed and part of ethyl acetate was evaporated, the crude product was purified by flash column chromatography (eluent: CH2Cl2:CH3Cl=1:1) to obtain the product as a glassy solid (0.20 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07304057B2
출처 데이터셋uspto-grants-2007_12
ORD IDord-b0edb37f230e4a95b95117548e185200
출처 메모uspto-grants-2007_12