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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874573Generated: October 29, 2026

Ethylacetate heptane → HCID 49847348, compound

https://huagongshe.com/reaction/874573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylacetate heptaneHCID 21899848—
ReactantHCID 49849201HCID 49849201—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 49847348HCID 4984734870%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980897B2
Source datasetuspto-grants-2015_03
ORD IDord-4651d8f7ed0e4919b3fae0064f4c50f2
Source noteuspto-grants-2015_03