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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 513829Generated: October 30, 2026

C20H17N3O3S → HCID 178432250, compound

https://huagongshe.com/reaction/513829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantC20H17N3O3SHCID 68005415—
ReactantHCID 178432278HCID 178432278—
SolventEthanolHCID 702—
ProductHCID 178432250HCID 17843225091%

Reaction Steps

(2-Methyl-1H-benzimidazol-5-yl)-hydrazine dihydrochloride (830 mg) was added to an ethanol solution (15 ml) of crude 2-(1-benzenesulfonyl-1H-indole-2-carbonyl)-3-dimethylamino acrylonitrile (1.17 g). The reaction mixture was heated with stirring under reflux for four hours. After cooling to room temperature, the mixture was allowed to stand at room temperature. The precipitated solid was collected by filtration, and washed with ethanol to give [5-amino-1-(2-methyl-1H-benzimidazol-5-yl)-1H-pyrazol-4-yl]-(1-benzenesulfonyl-1H-indol-2-yl)-methanone was obtained as a yellow solid (1.5 g, with a two-step yield of 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102692B2
Source datasetuspto-grants-2015_08
ORD IDord-20f8cec7771e43f1add9cb19dd175bc7
Source noteuspto-grants-2015_08