HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2399700Generated: October 25, 2026
Triethylamine → N-(1,1-Diethyl-prop-2-ynyl)-4-[4-(2-methoxy-phenyl)-piperazin-1-yl]-2-phenyl-butyramide
https://huagongshe.com/reaction/2399700
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Ethylpent-1-yn-3-amine | HCID 76710 | — |
| Reactant | 4-[4-(2-Methoxyphenyl)piperazin-1-yl]-2-phenylbutanoic acid | HCID 9863428 | — |
| Reactant | N,N-bis(2-oxo-3oxazolidinyl)phosphoramidic chloride | HCID 19975454 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(1,1-Diethyl-prop-2-ynyl)-4-[4-(2-methoxy-phenyl)-piperazin-1-yl]-2-phenyl-butyramide | HCID 15296374 | 26.8% |
Reaction Steps
A mixture of 4-[4-(2-methoxyphenyl)piperazin-1-yl]-2-phenylbutanoic acid (1.772 g, 5 mmole), triethylamine (1.518 g, 15 mmole), and N,N-bis(2-oxo-3-oxazolidinyl)phosphoramidic chloride (1.527 g, 6 mmole) was stirred in methylene chloride (80 mL) under exclusion of moisture at ambient temperature for 30 minutes, after which 1,1-diethylpropargylamine (0.668 g, 6 mmole) was added at once at 0° C. The reaction mixture was stirred at room temperature overnight, washed with water (2×100 mL), dried over magnesium sulfate, filtered, and evaporated to dryness in vacuo. Chromatography on silica gel with methanol/chloroform as eluant, followed by trituration from diethyl ether with addition of ethanolic hydrochloric acid gave 0.6 g of the title compound as the trihydrochloride hemihydrate, m.p. 110°-12° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05451584 |
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| Source dataset | uspto-grants-1995_09 |
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| ORD ID | ord-cf7ea46d5e13469ab5cf8bc2154f4afc |
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| Source note | uspto-grants-1995_09 |
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