HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Lutidine → HCID 131715955, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | tert-Butyldimethylsilyl trifluoromethanesulphonate | HCID 123564 | — |
| Reactant | Boc-L-Lys(Z)-OMe | HCID 11132998 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 131715955 | HCID 131715955 | — |
Reaction Steps
To a dichloromethane solution (1.0 ml) of Nα-t-butoxycarbonyl-Nε-benzyloxycarbonyllysine methyl ester (191.0 mg, 0.48 mmol) were added 2.6-lutidine (113 μl, 0.97 mmol) and t-butyldimethylsilyltrifluoromethane sulfonate (167 μl, 0.73 mmol). The mixture was stirred for 15 minutes in an argon atmosphere at room temperature. After addition of a saturated aqueous solution of ammonium chloride, the reaction mixture was extracted with ether and the ether layer was dried over anhydrous magnesium sulfate and filtered. After removal of the solvent in vacuo, Nα-butyldimethylsilyloxycarbonyl-Nε-benzyloxycarbonyllysine methyl ester was obtained (238 mg; yield, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04837349 |
| Source dataset | uspto-grants-1989_06 |
| ORD ID | ord-2cfa7d1b4fbc457dbe6bcb4b0fd3c358 |
| Source note | uspto-grants-1989_06 |