HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850897Generated: October 31, 2026
Ethylmorpholine → HCID 54201682, compound
https://huagongshe.com/reaction/850897
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylmorpholine | HCID 7525 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 54062324 | HCID 54062324 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 54201682 | HCID 54201682 | — |
Reaction Steps
0.5 ml of N-ethylmorpholine and 0.37 ml of acetic anhydride were added in sequence to a solution of 1.95 g of N-[N-[N-[N-(O-tert-butyl-L-seryl)-D-valyl]-2-methyl-L-phenylalanyl]-3-methyl-L-valyl]-L-leucine benzyl ester in 70 ml of anhydrous dichloromethane. The mixture was stirred at room temperature for 1 hour and was then washed in sequence with 5% aqueous citric acid solution, saturated aqueous sodium bicarbonate solution and saturated brine. The organic phase was dried over anhydrous magnesium sulphate and evaporated. Chromatography of the residue on silica using 5% methanol in dichloromethane for the elution gave afforded 1.45 g of N-[N-[N-[N-(N-acetyl-O-tert-butyl-L-seryl)-D-valyl]-2-methyl-L-phenylalanyl]-3-methyl-L-valyl]-L-leucine benzyl ester; MS: m/e 780.6 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06018020 |
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| Source dataset | uspto-grants-2000_01 |
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| ORD ID | ord-329ddc7e71454b478dbc83d4b1b08bbc |
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| Source note | uspto-grants-2000_01 |
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