HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Nitrobenzamide → 3-Nitrobenzylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Nitrobenzamide | HCID 12576 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Product | 3-Nitrobenzylamine | HCID 122722 | — |
Reaction Steps
Commercially available 3-nitrobenzamide is reduced with LAH under standard conditions to afford (3-nitrophenyl)methanamine, which is reacted with N-4-methoxybenzylsulfamic acid and EDC to afford 1-(4-methoxybenzyl)-3-benzylsulfonylurea. This material is reacted with oxalyl chloride to afford 1-(3-nitrobenzyl)-3-(4-methoxybenzyl)imidazolidine-2,2-dioxo-2-thio-4,5-trione whose nitro group is reduced and oxidized to afford 1-(3-hydrazinylbenzyl)-3-(4-methoxybenzyl)imidazolidine-2,2-dioxo-2-thio-4,5-trione. This material is deprotected with TFA under standard conditions to afford the title compound I-(3-hydrazinylbenzyl)imidazolidine-2,2-dioxo-2-thio-4,5-trione.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07737283B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-85310926569f41149255bdebe2e43fb0 |
| Source note | uspto-grants-2010_06 |