HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1777271Generated: October 31, 2026
Triethylamine → methyl (S)-3-(4-but-2-ynyloxybenzoylamino)-2-cyclohexylpropanoate
https://huagongshe.com/reaction/1777271
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 4-But-2-ynyloxy-benzoic acid | HCID 22282556 | — |
| Reactant | methyl (S)-3-amino-2-piperidin-1-ylpropanoate dihydrochloride | HCID 67494635 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | methyl (S)-3-(4-but-2-ynyloxybenzoylamino)-2-cyclohexylpropanoate | HCID 67056389 | 58% |
Reaction Steps
420 mg (3.1 mmol) of 1-hydroxybenzotriazole and 600 mg (3.1 mmol) of 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride are added to a solution of 540 mg (3.1 mmol) of 4-but-2-ynyloxybenzoic acid in 10 ml of dimethylformamide. The reaction medium is stirred for 15 min at ambient temperature then 630 mg (2.8 mmol) of methyl (S)-3-amino-2-piperidin-1-yl-propanoate dihydrochloride in 10 ml of dimethylformamide and 0.8 ml (5.7 mmol) of triethylamine are added. The reaction medium is stirred at ambient temperature for 18 h. The organic phase is washed with an aqueous solution of sodium hydrogen carbonate then with a saturated aqueous solution of sodium chloride, dried over magnesium sulphate, filtered and concentrated. The crude product obtained is purified by chromatography over silica gel eluted with a 99/1 dichloromethane/methanol mixture. 580 mg (58%) of methyl (S)-3-(4-but-2-ynyloxybenzoylamino)-2-cyclohexylpropanoate are obtained in the form of a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09266848B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-714ddae8c8644396931c40f533bc8b28 |
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| Source note | uspto-grants-2016_02 |
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