HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874573Generated: October 29, 2026
Ethylacetate heptane → HCID 49847348, compound
https://huagongshe.com/reaction/874573
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylacetate heptane | HCID 21899848 | — |
| Reactant | HCID 49849201 | HCID 49849201 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 49847348 | HCID 49847348 | 70% |
Reaction Steps
90 mg (0.15 mmol) of benzyl 4-((S)-1-hydroxycarbamoyl-2-[4-(2-methylquinolin-4-ylmethoxy)benzenesulfonylamino]ethyl)piperazine-1-carboxylate are placed in solution in 5 ml of dichloromethane and 5 ml of trifluoroacetic acid. The reaction medium is then stirred at ambient temperature for 96 h. After evaporation of the trifluoroacetic acid, the residue is taken up with 5 ml of saturated aqueous solution of sodium hydrogen carbonate and extracted with n-butanol. The organic phase is washed with water and then with a saturated aqueous solution of sodium chloride, dried over magnesium sulfate, filtered and concentrated under vacuum. The crude product obtained is taken up in a 50/50 heptane/ethyl acetate mixture, stirred for 1 h and then filtered and dried under vacuum. 50 mg (70%) of (S)-N-hydroxy-3-[4-(2-methylquinolin-4-ylmethoxy)benzenesulfonylamino]-2-piperazin-1-ylpropionamide are obtained in the form of a beige solid with a melting point of 225° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08980897B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-4651d8f7ed0e4919b3fae0064f4c50f2 |
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| Source note | uspto-grants-2015_03 |
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