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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256134Generated: October 25, 2026

2-Cyano-N-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)-4-nitrobenzenesulfonamide → HCID 67173422, compound

https://huagongshe.com/reaction/1256134

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Cyano-N-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)-4-nitrobenzenesulfonamideHCID 67174065—
CatalystNickelHCID 935—
SolventAmmonium hydroxide methanolHCID 21894508—
ProductHCID 67173422HCID 67173422100%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461134B2
Source datasetuspto-grants-2013_06
ORD IDord-bebd910f8da044c7b1d4ccbc4244f64b
Source noteuspto-grants-2013_06