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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352854Generated: November 3, 2026

Hydrochloric Acid → HCID 178426975, compound

https://huagongshe.com/reaction/2352854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl formateHCID 8025—
ReactantSodium ethoxideHCID 2723922—
Reactant2-tert-Butyl-5-methyl-2H-pyrazole-3-carboxylic acid [4-(2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amideHCID 86610395—
SolventEthanolHCID 702—
ProductHCID 178426975HCID 17842697581%

Reaction Conditions

Temperature78 °C

Reaction Steps

2-tert-Butyl-5-methyl-2H-pyrazole-3-carboxylic acid [4-(2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amide (0.634 g, 1.63 mmol) and ethyl formate (0.39 mL, 4.89 mmol) were dissolved in anhydrous ethanol (3.50 mL). The resulting solution was treated in dropwise fashion with a 21 wt % solution of sodium ethoxide in ethanol (3.05 mL, 8.16 mmol). This reaction mixture was heated at 78° C. for 1 h, producing a black oil. Subsequently, the reaction mixture was cooled to room temperature, and then the reaction pH was adjusted to pH 1 with dropwise addition of 1M HCl(aq) causing the formation of a pale orange precipitate. The suspension was filtered yielding an orange solid as the pure 2-tert-Butyl-5-methyl-2H-pyrazole-3-carboxylic acid [4-(3-hydroxymethylene-2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amide (0.548 g, 1.32 mmol, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07749530B2
Source datasetuspto-grants-2010_07
ORD IDord-6a7ab2d6f1eb482b9c3058ef32793af8
Source noteuspto-grants-2010_07