HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Benzamide,4-amino-n-(butylsulfonyl)-3-[[(2,4-dichlorophenyl)methyl]amino]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | N-1-butanesulfonyl-3-(2,4-dichlorobenzylamino)-4-nitrobenzamide | HCID 18315434 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzamide,4-amino-n-(butylsulfonyl)-3-[[(2,4-dichlorophenyl)methyl]amino]- | HCID 18315556 | 46.6% |
Reaction Steps
N-1-butanesulfonyl-3-(2,4-dichlorobenzylamino)-4-nitrobenzamide (0.505 g) was added to a mixture of 1.32 g of sodium hydrosulfite, 1 ml of ethanol, 1 ml of tetrahydrofuran and 1 ml of water at room temperature. The mixture was heat-refluxed for 40 minutes. The solvent was distilled off under reduced pressure, and water was added to the residue. The solid material precipitated was collected, and was dried. Further, the resulting material was washed with a mixed solution of 10 ml of methanol and 3 ml of water, and was dried to give 0.220 g of N-1-butanesulfonyl-4-amino-3-(2,4-dichlorobenzylamino)benzamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06166219 |
| Source dataset | uspto-grants-2000_12 |
| ORD ID | ord-873f4b8db2ff475ba97ad43cc7344377 |
| Source note | uspto-grants-2000_12 |