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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1463651Generated: October 31, 2026

Ethylmorpholine → FMOC-N-Me-Ser(O-Bzl)-Tyr-D-Leu-OEt

https://huagongshe.com/reaction/1463651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylmorpholineHCID 7525—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantFmoc-MeSer(Bzl)-OHHCID 44593820—
ReactantTyr-D-Leu-OEt hydrochlorideHCID 131717344—
SolventDimethylformamideHCID 6228—
ProductFMOC-N-Me-Ser(O-Bzl)-Tyr-D-Leu-OEtHCID 131717343—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of Tyr-D-Leu-OEt hydrochloride (1.649 g) in DMF (10 ml) cooled to 0° C. was added N ethylmorpholine (0.59 ml) in DMF (1 ml), followed by a solution of FMOC-N-Me-Ser(O-Bzl)-OH (2.18 g) in DMF (5 ml), followed by a solution of HOBt (0.9315 g) in DMF (5 ml), and followed by a solution of DCC (0.947 g) in DMF (2 ml). The reaction solution was stirred at 0° C. for 1 hour and then at room temperature for 4 hours. The solvent was removed in vacuo and the residue was purified by silica gel column chromatography eluting with (95:5) methylene chloride:methanol. The product was obtained as a semisolid. Rf 0.35. Fab Mass spec. m/e 736 (M+ +H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05300492
Source datasetuspto-grants-1994_04
ORD IDord-43351795ee2b4765b9e2d636edf3db5b
Source noteuspto-grants-1994_04