HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19247Generated: October 29, 2026
Diisopropylethylamine → HCID 66893768, compound
https://huagongshe.com/reaction/19247
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methyl 3-cyclohexyl-L-alaninate | HCID 13833920 | — |
| Reactant | HCID 66894842 | HCID 66894842 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 66893768 | HCID 66893768 | 16% |
Reaction Steps
To a stirred solution of (S)-2-amino-3-cyclohexyl-propionic acid methyl ester (1.05 g, 0.006 mol) in N,N-dimethylformamide (8 mL) was added N,N-diisopropylethylamine (3.30 g, 0.026 mol) slowly at room temperature, under nitrogen. The resulting mixture was stirred for 5 min and then treated with (E)-3-(2-benzyloxy-phenoxy)-4-bromo-but-2-enoic acid ethyl ester (2.00 g, 0.005 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)-2-[4-(2-benzyloxy-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-3-cyclohexyl-propionic acid methyl ester (360 mg, 14%) as a 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-cda728432e5c45bf905d4640d55af08b |
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| Source note | uspto-grants-2010_06 |
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