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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1406551Generated: October 26, 2026

Sodium Bicarbonate → 4-isopropoxy-N-(3-methyl-1-(quinolin-5-yl)-1H-pyrazol-5-yl)benzenesulfonamide

https://huagongshe.com/reaction/1406551

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant4-(Propan-2-yloxy)benzene-1-sulfonyl chlorideHCID 22327297—
Reactant3-methyl-1-(quinolin-5-yl)-1H-pyrazol-5-amineHCID 86694514—
SolventPyridineHCID 1049—
Product4-isopropoxy-N-(3-methyl-1-(quinolin-5-yl)-1H-pyrazol-5-yl)benzenesulfonamideHCID 717318328.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

A stirred mixture of 4-isopropoxybenzene-1-sulfonyl chloride (0.10 g, 0.52 mmol) and 3-methyl-1-(quinolin-5-yl)-1H-pyrazol-5-amine (prepared from Example 4 step b, 0.10 g, 0.44 mmol) in pyridine (2 mL) was heated at 80° C. for 1 h. After cooling to room temperature, aqueous saturated sodium bicarbonate was added to the reaction mixture and extracted with dichloromethane. The organic layer was dried (Na2SO4), filtered, and concentrated in vacuo. The crude residue was purified by flash chromatography (SiO2, 2-10% methanol in dichloromethane), followed by reverse phase HPLC(C18 column, acetonitrile-H2O with 0.1% TFA as eluent) to give the title compound as a white solid (0.015 g, 0.036 mmol, 8%). 1H NMR (400 MHz, CDCl3) δ 8.58 (dd, J=2.0, 4.0 Hz, 1H), 8.09 (d, J=8.4 Hz, 1H), 7.61 (dd, J=7.6, 8.4 Hz, 1H), 7.50 (d, J=2.0 Hz, 1H), 7.48 (d, J=1.6 Hz, 1H), 7.25-7.21 (m, 2H), 7.14 (dd, J=0.8, 7.2 Hz, 1H), 6.74 (d, J=2.4 Hz, 1H), 6.72 (d, J=2.0 Hz, 1H), 6.25 (s, 1H), 4.57 (hept, J=6.0 Hz, 1H), 2.33 (s, 3H), 1.39 (d, J=6.4 Hz, 6H); MS: (ES) m/z calculated for C23H23N4O3S [M+H]+ 423.2. found 423.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916601B2
Source datasetuspto-grants-2014_12
ORD IDord-1b85c7ee7a7b40558ba47cd4f5353939
Source noteuspto-grants-2014_12