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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227405Generated: October 30, 2026

Water → Ethyl[1-(4-aminosulfonylphenyl)-5-(4-chlorophenyl)-1H-pyrazole-3-yl]carboxylate

https://huagongshe.com/reaction/2227405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantmethyl 1-[4-(aminosulfonyl)phenyl]-5-(4-chlorophenyl)-1H-pyrazole-3-carboxylateHCID 3289819—
ReactantEthanol sodium ethoxideHCID 23706232—
SolventEthanolHCID 702—
ProductEthyl[1-(4-aminosulfonylphenyl)-5-(4-chlorophenyl)-1H-pyrazole-3-yl]carboxylateHCID 984422470%

Reaction Conditions

Temperature0 °C

Reaction Steps

Methyl [1-(4-aminosulfonylphenyl)-5-(4-chlorophenyl)-1H-pyrazole-3-yl]carboxylate (Example 85) (0.10 g) was dissolved in absolute ethanol (10 mL and a catalytic amount of 21% NaOEt/EtOH was added. The reaction was stirred without temperature control for 72 hours, then water (10 mL) was added. The product crystallized, the suspension was cooled to 0° C. and held for 30 minutes. The product was filtered, washed with water (5 mL) and dried to yield 0.071 g (70%) of a white solid: Mass Spectrum: MH+=406. Anal. Calc'd for C18H16N3O4ClS: C, 53.27; H, 3.97; N, 10.35; Cl, 8.74; S, 7.90. Found: C, 53.04; H, 4.00; N, 10.27; Cl, 8.69; s, 7.97.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06413960B1
Source datasetuspto-grants-2002_07
ORD IDord-e198e0c022d344dfa2a2939b5ae8fdf3
Source noteuspto-grants-2002_07