HuagongsheHuagongshe Chemistry Print Report · For research reference only
S-Trityl-L-Cysteine → 2(R)-[2,2,2-trifluoro-1(S)-(4-fluorophenyl)ethylamino]-3-tritylsulfanylpropionic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | S-Trityl-L-Cysteine | HCID 76044 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | trifluoromethanesulfonic acid 2,2,2-trifluoro-1(R)-(4-fluorophenyl)ethyl ester | HCID 86610096 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2(R)-[2,2,2-trifluoro-1(S)-(4-fluorophenyl)ethylamino]-3-tritylsulfanylpropionic acid | HCID 57562095 | 77.7% |
Reaction Steps
2(R)-Amino-3-tritylsulfanylpropionic acid (78 g, 214.6mmol) 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 IN 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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07488848B2 |
| Source dataset | uspto-grants-2009_02 |
| ORD ID | ord-b471f06108e047288c9f2aa40e01cdee |
| Source note | uspto-grants-2009_02 |