HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azetidine → N-[Azetidin-1-yl(methyl)oxo-lambda6-sulfanylidene]-4-bromoaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azetidine | HCID 10422 | — |
| Reactant | N-(4-Bromophenyl)methanesulfinamide | HCID 14195208 | — |
| Product | N-[Azetidin-1-yl(methyl)oxo-lambda6-sulfanylidene]-4-bromoaniline | HCID 118863933 | — |
Reaction Steps
The title compound is prepared from N-(4-bromophenyl)methanesulfinamide and azetidine following a procedure analogous to that described for Intermediate 3 (Step 2). LC (method 1): tR=0.92 min; Mass spectrum (ESI+): m/z=289, 291 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09422312B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-9e7e44c468b54107971b1c5ebc84ba9a |
| Source note | uspto-grants-2016_08 |