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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 642902생성일: 2026년 10월 25일

S-Trityl-L-Cysteine → 2(R)-[2,2,2-trifluoro-1(S)-(4-fluorophenyl)ethylamino]-3-tritylsulfanylpropionic acid

https://huagongshe.com/reaction/642902

반응식

참여 물질

역할이름HCID투입량
반응물S-Trityl-L-CysteineHCID 76044—
반응물DiisopropylethylamineHCID 81531—
반응물trifluoromethanesulfonic acid 2,2,2-trifluoro-1(R)-(4-fluorophenyl)ethyl esterHCID 86610096—
용매DichloromethaneHCID 6344—
생성물2(R)-[2,2,2-trifluoro-1(S)-(4-fluorophenyl)ethylamino]-3-tritylsulfanylpropionic acidHCID 5756209577.7%

반응 단계

2(R)-Amino-3-tritylsulfanylpropionic acid (78 g, 214.6 mmol) was dissolved in CH2Cl2 and DIPEA (112 mL, 643.8 mmol) was added and the reaction mixture was stirred for 10 min at room temperature. Trifluoromethanesulfonic acid 2,2,2-trifluoro-1(R)-(4-fluorophenyl)ethyl ester (70 g, 214.6 mmol) in CH2Cl2 was added and the reaction mixture was stirred overnight at room temperature. Solvent was removed under the reduced pressure and the residue was dissolved in Et2O and washed with 1N HCl, brine and dried over MgSO4. Solvent was removed give 2(R)-[2,2,2-trifluoro-1(S)-(4-fluorophenyl)ethylamino]-3-tritylsulfanylpropionic acid (90 g) as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07696250B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-5fb0d2de890f44ed9216088300ca49e7
출처 메모uspto-grants-2010_04