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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715834Generated: October 27, 2026

(4-{[1-(5-chloro-2-methoxy-benzenesulfonyl)-1H-indole-6-carbonyl]-amino}-phenyl)-acetic acid tert-butyl ester → (4-{[1-(5-Chloro-2-methoxy-benzenesulfonyl)-1H-indole-6-carbonyl]-amino}-phenyl)-acetic acid

https://huagongshe.com/reaction/1715834

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-{[1-(5-chloro-2-methoxy-benzenesulfonyl)-1H-indole-6-carbonyl]-amino}-phenyl)-acetic acid tert-butyl esterHCID 68432753—
SolventHydrochloric AcidHCID 313—
Solvent1,4-DioxaneHCID 31275—
Product(4-{[1-(5-Chloro-2-methoxy-benzenesulfonyl)-1H-indole-6-carbonyl]-amino}-phenyl)-acetic acidHCID 24962348—

Reaction Steps

(4-{[1-(5-Chloro-2-methoxy-benzenesulfonyl)-1H-indole-6-carbonyl]-amino}-phenyl)-acetic acid tert-butyl ester (0.25 g, 0.46 mmol) was dissolved in 4M HCl in dioxane (4.00 mL) and stirred at room temperature for 18 hours. The volatiles were evaporated and the residue taken up in ethyl acetate/heptane 1:1 and sonicated. The solid was filtered washing with ethyl acetate/heptane 1:1 and dried under vacuum. (4-{[1-(5-Chloro-2-methoxy-benzenesulfonyl)-1H-indole-6-carbonyl]-amino}-phenyl)-acetic acid was obtained as an off-white solid, 0.14 g (63%), MS (ISP): m/e=497.1 (M−H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799933B2
Source datasetuspto-grants-2010_09
ORD IDord-4a84fe0838614589b3cdbe857fff4172
Source noteuspto-grants-2010_09