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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1631986Generated: October 31, 2026

Water → HCID 66755192, compound

https://huagongshe.com/reaction/1631986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Methoxybenzenesulfonyl chlorideHCID 7401—
ReactantTriethylamineHCID 8471—
ReactantHCID 66754935HCID 66754935—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66755192HCID 66755192—

Reaction Steps

167 mg (0.81 mmol) of 4-methoxybenzenesulfonyl chloride were added to a solution of 460 mg (0.73 mmol) of tert-butyl 4-{4-[2-(6-chloro-2-oxo-2,3-dihydrobenzimidazol-1-yl)-2-phenylacetyl]-piperazin-1-yl}piperidin-1-carboxylate (XIIIa), 0.21 ml (1.47 mmol) of triethylamine and a catalytic amount of DMAP in tetrahydrofuran (8 ml) while stirring at room temperature, and the mixture was then stirred at room temperature for 16 h. The reaction solution was mixed with water and extracted with ethyl acetate (3×60 ml). The combined organic phases were washed with water and saturated brine, dried over magnesium sulfate and concentrated under reduced pressure. The residue was purified by chromatography on silica gel (mobile phase gradient 5-10% methanol in dichloromethane). Yield: 517 g (97%) of colorless oil

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791148B2
Source datasetuspto-grants-2014_07
ORD IDord-38628835e69f428ca8fcaad02d6763b3
Source noteuspto-grants-2014_07