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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651119Generated: October 31, 2026

5-cyano-1H-indole-2-carboxylic Acid → 5-Cyano-1H-indole-2-carboxylic acid ((1S)-benzyl-2-oxo-2-thiazolidin-3-yl-ethyl)-amide

https://huagongshe.com/reaction/651119

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-cyano-1H-indole-2-carboxylic AcidHCID 7144625—
Reactant(S)-2-Amino-3-phenyl-1-thiazolidin-3-yl-propan-1-one hydrochlorideHCID 69687431—
SolventHydrochloric AcidHCID 313—
SolventEthyl AcetateHCID 8857—
Product5-Cyano-1H-indole-2-carboxylic acid ((1S)-benzyl-2-oxo-2-thiazolidin-3-yl-ethyl)-amideHCID 57088889—

Reaction Steps

(S)-2-Amino-3-phenyl-1-thiazolidin-3-yl-propan-1-one hydrochloride (4.0 mmol) and 5-cyano-1H-indole-2-carboxylic acid (4.0 mmol) were coupled according to Procedure A (0-25° C. reaction temperature, 48 hours reaction time) with the following workup: the reaction mixture was diluted with ethyl acetate and 2 N HCl, the resulting precipitate collected by filtration, washed with 2 N HCl and 2 N NaOH. The crude product was purified by chromatography on silica gel eluted with 30, 40 and 60% ethyl acetate in hexanes. Yield 1.22 g, 75%; HPLC (60/40) 4.74 minutes (97%); PBMS 405 (MH+, 100%);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06277877B1
Source datasetuspto-grants-2001_08
ORD IDord-6fda81657fd44e429e1c7fb2788f9671
Source noteuspto-grants-2001_08