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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336221Generated: October 30, 2026

Phosphorus oxychloride → (S)-1-(4-Chloro-phenyl)-azepane-2-carboxylic acid (5-tert-butyl-isoxazol-3-yl)-amide

https://huagongshe.com/reaction/336221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactant3-Isoxazolamine, 5-(1,1-dimethylethyl)-HCID 171473—
Reactant(S)-1-(4-Chloro-phenyl)-azepane-2-carboxylic acidHCID 58563924—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
Product(S)-1-(4-Chloro-phenyl)-azepane-2-carboxylic acid (5-tert-butyl-isoxazol-3-yl)-amideHCID 58563918—

Reaction Steps

Phosphorus oxychloride (0.21 g, 1.38 mmol) is added drop wise at 0° C. to a solution of (S)-1-(4-chloro-phenyl)-azepane-2-carboxylic acid (0.23 g, 0.92 mmol) and 5-tert-butyl-isoxazol-3-ylamine (0.19 g, 1.38 mol) in pyridine. The reaction mixture is slowly warmed up to room temperature and stirred for three hours. The mixture is diluted with EtOAc and washed twice with saturated NH4Cl solution. The organic phase is washed with 1N HCl, and after drying over anhydrous Na2SO4 the solvent is removed under reduced pressure to afford the crude product that is purified by prep TLC to afford the title compound; m/z 376 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889670B2
Source datasetuspto-grants-2014_11
ORD IDord-91ee6462941743acab3a1cc25645ada1
Source noteuspto-grants-2014_11