Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | L-Tryptophan | HCID 6305 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 1,2-Ethanedithiol | HCID 10902 | — |
| Reactant | HCID 131723563 | HCID 131723563 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 131723565 | HCID 131723565 | 86.2% |
Reaction Steps
Under N2 atmosphere, the Boc-Aib-DTrp-DPro-diisobutylamide was dissolved in 30 ml of CH2Cl2, 1 ml of methylsulfide and 0.5 ml of 1,2-ethanedithiol were added as scavengers to suppress the indole alkylation of tryptophan. 10 ml of trifluoracetic acid was added dropwise while being stirred. The reaction mixture was stirred for 30 min. Volatiles were removed under vacuum and the residue was dissolved in 30 ml of CH2Cl2 and washed with 10 ml saturated NaHCO3 aqueous solution. The organic layer was removed and the aqueous layer was extracted with CH2Cl2 (3×10 ml). The organic layer was dried over anhydrous sodium sulfate, and filtered and the solvents were removed in vacuum. The residue was further purified by column chromatography (SiO2, CHCl/MeOH, 85:15) to afford 0.43 mmol (86.2%) of compound (YL-156) which was characterized by TLC and mass spectra M+=497.6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07250399B2 |
|---|
| Source dataset | uspto-grants-2007_07 |
|---|
| ORD ID | ord-bfc73910678c4c369c2e21727569262b |
|---|
| Source note | uspto-grants-2007_07 |
|---|