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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255343Generated: October 26, 2026

5-Fluoroindole-2-carboxylic acid → 5-Fluoro-N-{1-[2-(7-fluoro-2-oxoquinoxalin-1(2H)-yl)ethyl]piperidin-4-yl}-1H-indole-2-carboxamide

https://huagongshe.com/reaction/255343

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Fluoroindole-2-carboxylic acidHCID 1820—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant3-(Dimethylamino)propyl-ethyl-(iminomethylidene)azaniumHCID 21883392—
Reactant1-(2-(4-aminopiperidin-1-yl)ethyl)-7-fluoroquinoxalin-2(1H)-oneHCID 59397907—
Solventdichloromethane N,N-dimethylformamideHCID 22350042—
Product5-Fluoro-N-{1-[2-(7-fluoro-2-oxoquinoxalin-1(2H)-yl)ethyl]piperidin-4-yl}-1H-indole-2-carboxamideHCID 1598307379.6%

Reaction Steps

A mixture of 1-[2-(4-aminopiperidin-1-yl)ethyl]-7-fluoroquinoxalin-2(1H)-one (Intermediate 140, 130 mg, 0.448 mmol), 5-fluoro-1H-indole-2-carboxylic acid (96.3 mg, 0.538 mmol), N-(3-Dimethylaminopropyl)-N-ethylcarbodiimide (EDC)(124 mg, 0.645 mmol) and 1-Hydroxybenzotriazole hydrate (HOBT) (87 mg, 0.645 mmol) in dichloromethane/DMF (4:1, 10 mL) was stirred for 2.5 hours at room temperature. The solvent was removed under reduced pressure and the residue was suspended in methanol, stirred for 45 minutes and then filtered to give title compound (161 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875715B2
Source datasetuspto-grants-2011_01
ORD IDord-113c25239d61448faf92cc47a1cf30db
Source noteuspto-grants-2011_01