HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73875Generated: October 26, 2026
Diisopropylethylamine → N-[[1-[(2-Benzothienylcarbonyl)amino]cyclohexyl]carbonyl]-L-methionine methyl ester
https://huagongshe.com/reaction/73875
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | L-Methionine, methyl ester, hydrochloride | HCID 11435579 | — |
| Reactant | 2-(2-Benzothienyl)-3-oxa-1-azaspiro[4.5]dec-1-en-4-one | HCID 57672854 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-[[1-[(2-Benzothienylcarbonyl)amino]cyclohexyl]carbonyl]-L-methionine methyl ester | HCID 24739315 | 86.4% |
Reaction Steps
679 mg (5.3 mmol) of diisopropylethylamine was added to a suspension of 419 mg (2 mmol) of L-methionine methyl ester hydrochloride and 500 mg (1.75 mmol) of 2-(2-benzothienyl)-3-oxa-1-azaspiro[4.5]dec-1-en-4-one in 10 ml of toluene, and the mixture was heated under reflux overnight. After the solvent was distilled off under reduced pressure, ethyl acetate was added thereto, and the mixture was washed with a 10% aqueous potassium hydrogensulfate solution and saturated brine, followed by drying with anhydrous sodium sulfate. After the solvent was distilled off under reduced pressure, diethyl ether was added, and the mixture was stirred overnight. The precipitated solid was collected by filtration and dried under reduced pressure to obtain 678 mg (86%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08829209B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-db544b68519545c5a2c8df77955edff4 |
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| Source note | uspto-grants-2014_09 |
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