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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 908293Generated: October 30, 2026

Potassium Carbonate → N-(6-(2-oxoindolin-5-yl)naphthalen-2-yl)thiophene-3-carboxamide

https://huagongshe.com/reaction/908293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-DioxaneHCID 31275—
Reactant5-Bromo-2-oxindoleHCID 611193—
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-(2-oxoindolin-5-yl)naphthalen-2-yl)thiophene-3-carboxamideHCID 588288569%

Reaction Steps

5-bromoindolin-2-one (23.6 mg, 0.111 mmol), N-(6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalen-2-yl)thiophene-3-carboxamide (75.0 mg, 0.198 mmol), Fibercat palladium catalyst (Johnson-Matthey, 36.3 mg), and K2CO3 (2 M in water, 0.25 ml, 0.5 mmol) were combined in a microwave reaction vessel and 1,4-dioxane (1.1 ml) was added. The reaction tube was sealed and heated in the microwave (CEM microwave) at 60 Watts and 80 C, first for 10 minutes, and then for 20 minutes. The reaction was cooled to room temperature, diluted with water (5 ml), and extracted with dichloromethane (3×10 ml) and EtOAc (6×10 ml). The organic extracts were combined, dried over sodium sulfate, filtered, concentrated, and purified two times on HPLC (10%->95% MeCN/water with 0.1% TFA) to afford title compound (3.8 mg, 9%). MS (ESI pos. ion) m/z: 385 (M+H). Calc'd Exact Mass for C23H16N2O2S: 384.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08017601B2
Source datasetuspto-grants-2011_09
ORD IDord-9aa4e067ac694de0a143e1752e38aa4d
Source noteuspto-grants-2011_09