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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1622164Generated: November 1, 2026

HCID 178511956, compound → HCID 178511954, compound

https://huagongshe.com/reaction/1622164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178511956HCID 178511956—
CatalystAdams' catalystHCID 345198—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 178511954HCID 17851195435.6%

Reaction Steps

2-[2-Hydroxy-3′-nitro-5-(3-pyridin-3-yl-propionylsulfamoyl)-biphenyl-3-yl]-1H-benzoimidazole-5-carboxamidine (0.031 g, 0.05 mMol), prepared as in Example 10, was dissolved in trifluoroacetic acid (5 mL) and the solution was subjected to hydrogenation at 50 psi over PtO2 catalyst for 12 hours. The mixture was concentrated in vacuum and product was purified from the residue by reverse phase HPLC (acetonitrile gradient) to give 2-[3′-amino-2-hydroxy-5-(3-piperidin-3-yl-propionylsulfamoyl)-biphenyl-3-yl]-1H-benzoimidazole-5-carboxamidine (0.01 g). MS: found (M+H+) 562.4, (M−H+) 560.6, calc. 561.22.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778625B2
Source datasetuspto-grants-2014_07
ORD IDord-5c56c3d31d4746139a79c7ab6dd842c2
Source noteuspto-grants-2014_07