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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445232Generated: October 30, 2026

Glyoxal → HCID 178510411, compound

https://huagongshe.com/reaction/1445232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlyoxalHCID 7860—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 178510410HCID 178510410—
SolventDichloromethaneHCID 6344—
ProductTrifluoroacetic acidHCID 64220.1%
ProductHCID 178510411HCID 17851041119%

Reaction Steps

A suspension of 4-cyano-1H-imidazole-2-carboxylic acid {4-[1-(2-amino-acetyl)-piperidin-4-yl]-2-cyclohex-1-enyl-phenyl]-amide trifluoroacetic acid salt (as prepared in the previous step, 0.42 g, 0.77 mmol) in CH2Cl2 (20 mL) was treated with Na(OAc)3BH (0.33 g, 1.54 mmol) and solid glyoxal (44.6 mg, 0.77 mmol). The mixture stirred at room temperature for 1 h, and the solvent was evaporated in vacuo. The residue was taken up in MeOH and the solids filtered off, and the filtrate was concentrated in vacuo. Reverse phase HPLC (C-18 column) (20% to 60% acetonitrile in water with 0.1% TFA over 30 min) afforded the title compound (83 mg, 19% over two steps) as a white solid. 1H-NMR (CD3OD; 400 MHz): δ 8.16-8.09 (m, 1H), 8.05-8.01 (m, 1H), 7.22-7.15 (m, 1H), 7.11-7.06 (m, 1H), 5.84-5.79 (m, 1H), 4.72-4.62 (m, 1H), 4.24-3.91 (m, 2H), 3.89-3.80 (m, 2H), 3.28-3.18 (m, 2H), 2.92-2.79 (m, 2H), 2.28 (br s, 4H), 1.98-1.89 (m, 2H), 1.89-1.76 (m, 4H), 1.76-1.57 (m, 2H). LC-MS (ESI, m/z): Calcd. for C26H32N6O3 477.2 (M+H), found 477.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662837B2
Source datasetuspto-grants-2010_02
ORD IDord-e9e52d8625da4ec69d42824923b4cad2
Source noteuspto-grants-2010_02