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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802431Generated: November 3, 2026

Bromhydrol → HCID 178454507, compound

https://huagongshe.com/reaction/1802431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromhydrolHCID 166749—
ReactantHCID 178489123HCID 178489123—
SolventEthanethiolHCID 6343—
ProductHCID 178454507HCID 17845450739.3%

Reaction Steps

To a solution of 118 mg (0.29 mmol) of N-[5-(4-Methoxy-phenyl)-4H-[1,2,4]triazol-3-yl]-2-methyl-2-(tetrahydro-pyran-4-sulfonyl)-propionamide in ethanethiol (5 mL) are added 750 mg (2.9 mmol) of aluminium tribromide. The reaction is stirred at room temperature for 20 h. The reaction is quenched by addition of 12M aqueous HCl solution (2 mL) and diluted with water (10 mL). The aqueous layer is extracted with ethyl acetate (3×20 mL). The combined organic extracts are dried over Na2SO4, filtered and the filtrate is concentrated under reduced pressure. The residual solid is washed with DCM to afford 45 mg of N-[5-(4-hydroxy-phenyl)-4H-[1,2,4]triazol-3-yl]-2-methyl-2-(tetrahydro-pyran-4-sulfonyl)-propionamide. Yield: 38%, ES-MS: m/z 395 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349871B2
Source datasetuspto-grants-2013_01
ORD IDord-2ed048d9493f45daba785a6246babd3c
Source noteuspto-grants-2013_01