HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Boc-Tyr(OBn)-Ser(OBn)-CO2Me
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | O-benzyl-N-((tert-butoxy)carbonyl)-L-tyrosine | HCID 98763 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | Ser(OBn)-CO2Me.TFA | HCID 131720920 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Boc-Tyr(OBn)-Ser(OBn)-CO2Me | HCID 131720919 | 73% |
Reaction Steps
To a solution of Boc-Tyr(OBn) (1.88 g, 6.50 mmol) in EtOAc (30 mL) at 0° C. was added HOBT hydrate (1.19 g, 7.80 mmol) followed by DCC (1.61 g, 7.80 mmol). A solution of Ser(OBn)-CO2Me.TFA (2.1 g, 6.50 mmol) in EtOAc (20 mL) was added followed by Et3N (1.09 mL, 7.80 mmol). The mixture was allowed to warm to room temperature and stirred overnight. The mixture was filtered, diluted with EtOAc, and washed twice with saturated aqueous NaHCO3, brine, dried over MgSO4, and concentrated. Flash chromatography (40% EtOAc/hexane) gave 2.67 g (73%) of the title compound as a white solid, mp 81°-84° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05830868 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-b912eaba23384d21b5d4e1751cf41837 |
| Source note | uspto-grants-1998_11 |