HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19237Generated: October 25, 2026
Diisopropylethylamine → HCID 66895016, compound
https://huagongshe.com/reaction/19237
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methyl 3-cyclohexyl-L-alaninate | HCID 13833920 | — |
| Reactant | HCID 66894821 | HCID 66894821 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 66895016 | HCID 66895016 | 15.2% |
Reaction Steps
To a stirred solution of (S)-2-amino-3-cyclohexyl-propionic acid methyl ester (750 mg, 0.004 mol) in N,N-dimethylformamide (10 mL) was added N,N-diisopropylethylamine (2.6 g, 0.02 mol) slowly at room temperature, under nitrogen. The resulting mixture was stirred for 5 min and then treated with (E)-4-bromo-3-(2,5-dichloro-phenoxy)-but-2-enoic acid ethyl ester (1.5 g, 0.004 mol) and the reaction mixture was heated at 110° C.-120° C. for 16 h. After this time, ice water was added and the resulting mixture was extracted with ethyl acetate. The combined organic layers were washed with a saturated aqueous sodium chloride solution, dried over sodium sulfate and concentrated in vacuo. Purification by flash column chromatography (silica gel (100-200 mesh)) afforded (S)-3-cyclohexyl-2-[4-(2,5-dichloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-propionic acid methyl ester (250 mg, 15%) as yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07741327B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-759a56c5ccc54e19b7dfec9c989cc7fe |
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| Source note | uspto-grants-2010_06 |
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