Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
S-Trityl-L-Cysteine → 2(R)-[2,2,2-trifluoro-1(S)-(4-fluorophenyl)ethylamino]-3-tritylsulfanylpropionic acid
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | S-Trityl-L-Cysteine | HCID 76044 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | trifluoromethanesulfonic acid 2,2,2-trifluoro-1(R)-(4-fluorophenyl)ethyl ester | HCID 86610096 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 2(R)-[2,2,2-trifluoro-1(S)-(4-fluorophenyl)ethylamino]-3-tritylsulfanylpropionic acid | HCID 57562095 | 77.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07696250B2 |
| 출처 데이터셋 | uspto-grants-2010_04 |
| ORD ID | ord-5fb0d2de890f44ed9216088300ca49e7 |
| 출처 메모 | uspto-grants-2010_04 |