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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2280117Generated: November 2, 2026

Chlorosulfamic acid → (S)-2-sulfamoylamino-6-((1-butyrylpiperidin-3-yl)methoxy)benzonitrile

https://huagongshe.com/reaction/2280117

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfamic acidHCID 24499—
Reactant(S)-2-amino-6-((1-butyrylpiperidin-3-yl)methoxy)benzonitrileHCID 86714268—
SolventDimethylacetamideHCID 31374—
Product(S)-2-sulfamoylamino-6-((1-butyrylpiperidin-3-yl)methoxy)benzonitrileHCID 8671426782%

Reaction Steps

To a solution of (S)-2-amino-6-((1-butyrylpiperidin-3-yl)methoxy)benzonitrile (Example 1b, 9.2 g, 30.53 mmol) in DMA (60 mL) was added sulfamoyl chloride (Example 1f, 10.54 g, 91.58 mmol) at room temperature under nitrogen. The reaction mixture was stirred at room temperature under nitrogen overnight then concentrated under reduced pressure, diluted with EtOAc, successively washed with NaHCO3, water and brine, dried over Na2SO4, filtered and the solvent was removed under reduced pressure to give the title compound as colorless gel (9.5 g) in 82% yield. MS 381 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09138013B2
Source datasetuspto-grants-2015_09
ORD IDord-1bfc87a9e7a3405c9212837fc38d2361
Source noteuspto-grants-2015_09