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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024984Generated: October 29, 2026

Sulfamide → 3-(tert-Butyl-diphenyl-silanyloxy)-azetidine-1-sulfonamide

https://huagongshe.com/reaction/1024984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfamideHCID 82267—
Reactant3-((Tert-butyldiphenylsilyl)oxy)azetidineHCID 17842531—
Solvent1,4-DioxaneHCID 31275—
Product3-(tert-Butyl-diphenyl-silanyloxy)-azetidine-1-sulfonamideHCID 67051247—

Reaction Steps

The subtitle compound was prepared according to the procedure outlined in example 15 step (i) using 3-(tert-butyl-diphenyl-silanyloxy)-azetidine (prepared according to patent WO 2003/072557) (0.93 g), dioxane (20 ml) and sulfamide (0.34 g). Isolation was by filtration to remove excess sulfamide, the filtrate was then reduced in vacuo to give the subtitle compound as a brown oil. Yield: 1.2 g

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722883B2
Source datasetuspto-grants-2014_05
ORD IDord-78545953344a4b319227c4e0dbd927a4
Source noteuspto-grants-2014_05