HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890926Generated: October 27, 2026
4-Methylmorpholine → N-(benzylsulfonyl)-D-isoleucyl-L-methionine methyl ester
https://huagongshe.com/reaction/890926
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | L-Methionine, methyl ester, hydrochloride | HCID 11435579 | — |
| Reactant | N-(benzylsulfonyl)-D-isoleucine | HCID 36688801 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(benzylsulfonyl)-D-isoleucyl-L-methionine methyl ester | HCID 69623705 | 67.1% |
Reaction Steps
To a solution of N-(benzylsulfonyl)-D-isoleucine (6.3 g, 22.2 mmol) and L-methionine methyl ester hydrochloride (6.7 g, 33.3 mmol) in dichloromethane (100 ml), HOBt (4.1 g, 26.6 mmol), EDC HCl (5.1 g, 1.2 mmol) and N-methylmorpholine (3.4 g, 33.3 mmol) were added and stirred at room temperature under a nitrogen stream. After 12 hours, water was added to the reaction mixture, which was then extracted with ethyl acetate. The ethyl acetate layer was washed sequentially with 10% aqueous citric acid, saturated aqueous sodium bicarbonate and saturated brine, and then dried over anhydrous magnesium sulfate. After magnesium sulfate was filtered off, the filtrate was concentrated under reduced pressure and the residue was applied to flash column chromatography (Merck Silicagel 60; mobile phase: dichloromethane) to give N-(benzylsulfonyl)-D-isoleucyl-L-methionine methyl ester (6.4 g, 14.9 mmol; yield 67%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07001887B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-9b33fd25ae764fea9b46b84287d2df49 |
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| Source note | uspto-grants-2006_02 |
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