HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 10171560, compound → HCID 10171430, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 10171560 | HCID 10171560 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 10171430 | HCID 10171430 | — |
Reaction Steps
To a solution of the title C compound in Example 5, 5-(3-nitrobenzyl)-1,1-dioxo-1,2,5-thiadiazolidin-3-one (30 mg, 0.11 mmol) in EtOH (5 mL) is added palladium on carbon (10 mg) and the mixture is stirred under 1 atm of hydrogen for 1 h. The catalyst is removed by filtration through a plug of Celite which is washed with MeCN/water (1:1), (20 mL). The solvents are evaporated to afford 5-(3-Aminobenzyl)-1,1-dioxo-1,2,5-thiadiazolidin-3-one as a brown solid: [M−1]−=240.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07291635B2 |
| Source dataset | uspto-grants-2007_11 |
| ORD ID | ord-69f3f3c1e8a84171857021c18c2e4a16 |
| Source note | uspto-grants-2007_11 |