HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799231Generated: October 31, 2026
Ethyl Acetate → 4-(2-Cyclopropylethoxy)-n-[2-[(2-hydroxyethyl)amino]-2-oxo-1-(4-propylbenzyl)ethyl]benzamide
https://huagongshe.com/reaction/1799231
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | MeOH tetrahydrofuran | HCID 21899815 | — |
| Reactant | 4-(2-Cyclopropylethoxy)-N-((Z)-2-(4-cyclopropylphenyl)-1-{[(2-hydroxyethyl)amino]carbonyl}vinyl)benzamide | HCID 57684560 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Acetonitrile--water (1/1) | HCID 18373917 | — |
| Product | 4-(2-Cyclopropylethoxy)-n-[2-[(2-hydroxyethyl)amino]-2-oxo-1-(4-propylbenzyl)ethyl]benzamide | HCID 57972150 | 48% |
Reaction Steps
To a methanol:THF (2:1, V/V, 6 mL) solution of 4-(2-cyclopropylethoxy)-N-((Z)-2-(4-cyclopropylphenyl)-1-{[(2-hydroxyethyl)amino]carbonyl}vinyl)benzamide (215 mg, 0.495 mmol) prepared in Example (1 (1d) was added 10% palladium-carbon (wet, 100 mg). The mixture was stirred under a hydrogen atmosphere (rubber balloon) at room temperature for 2 hours. To the reaction solution was added ethyl acetate (10 mL), and the mixture was filtered. The solvent was evaporated, and the residue was purified by thin layer chromatography for separation (ethyl acetate, developed once) to give a white solid. This solid was suspended in acetonitrile:water (1:1, V/V, 4 mL), and the insoluble substance was collected by filtration, washed with water, and dried under reduced pressure to give 104 mg of the title compound (white powder, yield: 48%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08344029B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-ae221d732ef046aa8db736f06f6c914f |
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| Source note | uspto-grants-2013_01 |
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