HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(4-(N-cyano-S-methylsulfonimidoyl)benzyl)isoindoline-1,3-dione → 2-(5-(N-Cyano-S-methylsulfonimidoyl)pyridin-2-yl)-isoindole-1,3-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(4-(N-cyano-S-methylsulfonimidoyl)benzyl)isoindoline-1,3-dione | HCID 86711610 | — |
| Reactant | HCID 86711626 | HCID 86711626 | — |
| Product | 2-(5-(N-Cyano-S-methylsulfonimidoyl)pyridin-2-yl)-isoindole-1,3-dione | HCID 86711625 | — |
Reaction Steps
The title compound is prepared in analogy to preparation 6c, substituting 2-(4-(N-cyano-S-methylsulfinimidoyl)benzyl)isoindoline-1,3-dione with 2-(5-(N-cyano-S-methylsulfinimidoyl)pyridin-2-yl)-isoindole-1,3-dione (preparation 16c). ESI mass spectrum: [M+H]+=341; r.t. HPLC: 0.88 min (Z018_S04).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09346794B1 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-dc048a09b9174a9199efc02fb2bec3b0 |
| Source note | uspto-grants-2016_05 |