HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167107Generated: October 25, 2026
Triethylamine → Methyl 2-methyl-2-phenyl-5-{4-[(biphenyl-2-carbonyl)-amino]-piperidin-1-yl}-pentanecarboxylate
https://huagongshe.com/reaction/1167107
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-[(2-Biphenyl)carbonylamino]piperidine | HCID 11391851 | — |
| Reactant | Methyl 5-bromo-2-methyl-2-phenyl-pentanecarboxylate | HCID 22995606 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-methyl-2-phenyl-5-{4-[(biphenyl-2-carbonyl)-amino]-piperidin-1-yl}-pentanecarboxylate | HCID 22995520 | — |
Reaction Steps
A solution of 0.634 g (0.002 mol) of biphenyl-2-carboxylic acid-piperidin-4-ylamide, 0.5 g (1.75 mmol) of methyl 5-bromo-2-methyl-2-phenyl-pentanecarboxylate and 1 ml (0.007 mol) of triethylamine are dissolved in 3 ml dimethylformamide. The mixture is stirred for 14 hours at 80° C. Then the reaction mixture is poured onto water and extracted with ethyl acetate. The organic phase is dried over sodium sulphate. After column chromatography on silica gel (eluant: dichloromethane/methanol=10:1) colourless crystals remain.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06617325B1 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-be0aaedc435e4e1c9fd25e02e5d8de5a |
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| Source note | uspto-grants-2003_09 |
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