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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1163420Generated: October 23, 2026

Glyoxylic Acid → HCID 178525831, compound

https://huagongshe.com/en/reaction/1163420

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlyoxylic AcidHCID 760—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 178478620HCID 178478620—
CatalystAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 178525831HCID 178525831—

Reaction Steps

To a solution of 6-piperazin-1-yl-2-(2-trifluoromethylphenylamino)-1H-benzimidazole-5-carboxylic acid (1H-indazol-6-yl)-amide trihydrochloride (0.25 mmol; see Example 88) in methanol (1 mL) was added glyoxylic acid (0.5 mmol), and the resulting mixture was stirred at RT for 60 min. The reaction mixture was then charged with solid sodium cyanoborohydride (0.6 mmol), and the stirring was continued at RT for 10 h. To the reaction mixture was then added a few drops of glacial acetic acid, and the mixture was stirred for 30 min. The volatiles were then removed in vacuo, and the residue was suspended in water (10 mL) with vigorous stirring. After 30 min, the solid was filtered, washed with water, and dried under vacuum to afford {4-[6-(1H-indazol-6-ylcarbamoyl)-2-(2-trifluoromethyl-phenylamino)-3H-benzoimidazol-5-yl]-piperazin-1-yl}acetic acid as a white solid. MS: m/z 579 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820821B2
Source datasetuspto-grants-2010_10
ORD IDord-7b7f6090563e4b9ea11e5b7f17ef1115
Source noteuspto-grants-2010_10