Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873662Generated: October 31, 2026

HCID 58107424, compound → HCID 58107463, compound

https://huagongshe.com/reaction/873662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 58107424HCID 58107424—
SolventMethanolHCID 887—
SolventSodium HydroxideHCID 14798—
ProductHCID 58107463HCID 5810746366%

Reaction Steps

5-(1-Benzenesulfonyl-1H-pyrrole-3-carbonyl)-2-chloro-benzenesulfonamide (0.1 g, 0.23 mmol) is dissolved in 3 mL of 2:1 (v:v) mixture of methanol and 5 N aqueous sodium hydroxide and heated at reflux for 20 minutes then the reaction mixture is allowed to cool down and the organic solvent is removed in vacuo. The aqueous solution is acidified with 5 N HCl to pH 3, thoroughly extracted with ethyl acetate, then the combined organic extracts are washed with water, a saturated sodium chloride solution, dried with magnesium sulfate, and concentrated in vacuo. Recrystallization from ethyl acetate/methylene chloride provides 43 mg (66%) of the title compound as a white solid. 1H NMR (DMSO): δ 11.70 (s, 1H), 8.70 (m, 1H), 8.00 (m, 1H), 7.80 (m, 3H), 7.50 (m, 1H), 7.00 (m, 1H), 6.60 (m, 1H). MS (m/z): 285 (M+1) Analytics calculated For C11H9N2ClO3S: C, 46.40; H, 3.19; N, 9.84. Found: C, 45.84; H, 2.90; N, 9.41.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975439B2
Source datasetuspto-grants-2015_03
ORD IDord-c0d28466e80c4a86959b6bc839209d4b
Source noteuspto-grants-2015_03