HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 3,4-diamino-N-(cyclopentyloxy)benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 4-amino-N-(cyclopentyloxy)-3-nitrobenzenesulfonamide | HCID 22997190 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3,4-diamino-N-(cyclopentyloxy)benzenesulfonamide | HCID 22997182 | 100.7% |
Reaction Steps
A solution of 4-amino-N-(cyclopentyloxy)-3-nitrobenzenesulfonamide (4.50 g, 14.95 mmol) in 1:1 ethyl acetate:ethanol (150 mL) was combined with 5% Pd on barium sulfate and reduced under a hydrogen atmosphere over 72 hours. The reaction mixture was filtered through a pad of diatomaceous earth and evaporated in vacuo to a residue which crystallized on standing. The solid was slurried in hexane, filtered and dried under high vacuum to provide 3,4-diamino-N-(cyclopentyloxy)benzenesulfonamide (4.086 g, 100%) as a light brown solid H1-NMR (dimethylsulfoxide-D6): 1.61 (m, 8H), 4.37 (m, 1H), 4.90 (b, 2H), 5.38 (b, 2H), 6.57 (d, 1H), 6.88 (m, 1H), 6.96 (d, 1H), 9.64 (s, 1H). MS(ESI): 272(M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07419967B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-13dbb797a45142c6b9b7401d41f37a77 |
| Source note | uspto-grants-2008_09 |