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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 908300Generated: October 31, 2026

Potassium Carbonate → N-[6-(1H-Indol-5-yl)naphthalen-2-yl]thiophene-3-carboxamide

https://huagongshe.com/reaction/908300

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant5-BromoindoleHCID 24905—
Reactant1,4-DioxaneHCID 31275—
ReactantN-(6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalen-2-yl)thiophene-3-carboxamideHCID 67386422—
CatalystPalladiumHCID 23938—
SolventWaterHCID 962—
ProductN-[6-(1H-Indol-5-yl)naphthalen-2-yl]thiophene-3-carboxamideHCID 5882886021%

Reaction Steps

5-bromo-1H-indole (31.4 mg, 0.160 mmol), N-(6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalen-2-yl)thiophene-3-carboxamide (114 mg, 0.301 mmol), Fibercat palladium catalyst (Johnson-Matthey, 31 mg), and K2CO3 (2 M in water, 0.45 ml, 0.90 mmol) were combined in a microwave reaction vessel and 1,4-dioxane (1.5 ml) was added. The reaction tube was sealed and heated in the microwave (CEM microwave) at 60 Watts and 80 C for 20 minutes. The reaction was cooled to room temperature, diluted with water (5 ml), and extracted with EtOAc (3×10 ml). The organic extracts were combined, dried over sodium sulfate, filtered, concentrated, and purified on silica gel (5:1->4:1->2:1 hexanes/EtOAc) to afford crude product. This crude material was then purified two times via HPLC (10%->95% MeCN/water with 0.1% TFA) afford title compound (12.2 mg, 21%). MS (ESI pos. ion) m/z: 369 (M+H). Calc'd Exact Mass for C23H16N2OS: 368.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08017601B2
Source datasetuspto-grants-2011_09
ORD IDord-c986e6e4b9b149af994f51f451873ebe
Source noteuspto-grants-2011_09