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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 553644Generated: November 1, 2026

Bromhydrol → HCID 178454507, compound

https://huagongshe.com/reaction/553644

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 numberUS08048899B2
Source datasetuspto-grants-2011_11
ORD IDord-88f1c31e943b4215bce216d4a6e7e26d
Source noteuspto-grants-2011_11