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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1483929Generated: October 31, 2026

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

https://huagongshe.com/reaction/1483929

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 numberUS09420814B2
Source datasetuspto-grants-2016_08
ORD IDord-8a66fca4db0349ccbce6c077d99ad44a
Source noteuspto-grants-2016_08