HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Cyano-N-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)-4-nitrobenzenesulfonamide → HCID 67173422, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Cyano-N-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)-4-nitrobenzenesulfonamide | HCID 67174065 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ammonium hydroxide methanol | HCID 21894508 | — |
| Product | HCID 67173422 | HCID 67173422 | 100% |
Reaction Steps
To a solution of 2-cyano-N-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)-4-nitrobenzenesulfonamide (1.077 g, 3 mmol) in MeOH/NH4OH (100 ml/10 ml) was added Raney Ni (2 g) under nitrogen, then the solution was stirred under hydrogen atmosphere at room temperature for overnight. The mixture was filtered and the filtrate was concentrated to give title compound 4-amino-2-(aminomethyl)-N-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)benzenesulfonamide (1.0 g, 100%) as a green solid. 1H NMR: DMSO 400 MHz. δ7.41 (d, J=14.0 Hz, 2H), 7.16 (d, J=8.0 Hz, 1H), 7.08 (d, J=8.0 Hz, 1H), 6.63 (s, 1H), 6.33 (d, J=8.4 Hz, 1H), 5.82 (brs, 2H), 4.84 (s, 2H), 3.95 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08461134B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-bebd910f8da044c7b1d4ccbc4244f64b |
| Source note | uspto-grants-2013_06 |