HuagongsheHuagongshe Chemistry Print Report · For research reference only
(4-(N-cyano-S-methylsulfonimidoyl)phenyl)methanamine → (4-(N-Cyano-S-isopropylsulfonimidoyl)phenyl)methanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (4-(N-cyano-S-methylsulfonimidoyl)phenyl)methanamine | HCID 86711611 | — |
| Reactant | 2-(4-(N-cyano-S-isopropylsulfonimidoyl)benzyl)isoindoline-1,3-dione | HCID 86711619 | — |
| Product | (4-(N-Cyano-S-isopropylsulfonimidoyl)phenyl)methanamine | HCID 86711620 | — |
Reaction Steps
The title compound is prepared in analogy to preparation 6d, substituting 2-(4-(N-cyano-S-methylsulfonimidoyl)benzyl)isoindoline-1,3-dione with 2-(4-(N-cyano-S-isopropylsulfonimidoyl)benzyl)isoindoline-1,3-dione (preparation 14b). ESI mass spectrum: [M+H]+=238; r.t. HPLC: 0.59 min (Z011_S03).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09346794B1 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-506d17c228474aeb8ade338f58638709 |
| Source note | uspto-grants-2016_05 |