HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfamide → 3-(tert-Butyl-diphenyl-silanyloxy)-azetidine-1-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfamide | HCID 82267 | — |
| Reactant | 3-((Tert-butyldiphenylsilyl)oxy)azetidine | HCID 17842531 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-(tert-Butyl-diphenyl-silanyloxy)-azetidine-1-sulfonamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08722883B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-78545953344a4b319227c4e0dbd927a4 |
| Source note | uspto-grants-2014_05 |