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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylmorpholine | HCID 7525 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Fmoc-MeSer(Bzl)-OH | HCID 44593820 | — |
| Reactant | Tyr-D-Leu-OEt hydrochloride | HCID 131717344 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | FMOC-N-Me-Ser(O-Bzl)-Tyr-D-Leu-OEt | HCID 131717343 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05300492 |
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| Source dataset | uspto-grants-1994_04 |
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| ORD ID | ord-43351795ee2b4765b9e2d636edf3db5b |
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| Source note | uspto-grants-1994_04 |
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