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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106657Generated: November 1, 2026

HCID 18789771, compound → HCID 54465196, compound

https://huagongshe.com/reaction/1106657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18789771HCID 18789771—
ReactantHCID 22048993HCID 22048993—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54465196HCID 54465196—

Reaction Steps

To a solution of 1-[(2-amino-ethyl)-amino]-4-cyano-4-phenylhexane (25 mg, 0.103 mmol) in 10 mL of THF, 4-(3,4,5-trifluorophenyl)-2-oxo-oxazolidine-3-carboxylic acid-4-nitro-phenyl ester (30 mg, 0.079 mmol) was added and the resulting yellow solution was stirred under argon atmosphere for 2 h at room temperature. The solvent was removed in vacuo and the residue was purified by column chromatography over silica gel with 1:1 hexane/EtOAc followed by MeOH:EtOAc=1:9 (Rf =0.60, MeOH:EtOAc=1:3) to obtain the title compound. The compound was dissolved in CH2Cl2 (3 mL) and was treated with 1N HCl in ether (1 mL). The solvent was removed in vacuo to give the corresponding hydrochloride salt as a pale yellow solid. M. P. 130-134° C.; [α]D =+43.5, (c=0.25, MeOH); Anal. Calcd. For C25H26N4O3F3Cl 1.10 C3H6O: C, 57.92; H, 5.60; N, 8.55. Found: C, 58.33; H, 5.90; N, 8.52.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06057350
Source datasetuspto-grants-2000_05
ORD IDord-e8c226a325a3479a97e044ff7de21f1a
Source noteuspto-grants-2000_05