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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474139Generated: October 30, 2026

Sodium Carbonate → HCID 59299295, compound

https://huagongshe.com/reaction/474139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant5-Indolylboronic acidHCID 2734361—
ReactantHCID 66679914HCID 66679914—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventToluene ethanolHCID 21863594—
ProductHCID 59299295HCID 5929929567%

Reaction Conditions

Temperature90 °C

Reaction Steps

5.19 g (17.4 mmol) of (4S,5R)-4-(5-bromo-pyrimidin-2-yloxy)-1-aza-bicyclo[3.3.1]nonane is dissolved in 200 ml toluene/EtOH 9:1. 5-Indolyl boronic acid (3.47 g, 21.6 mmol), Pd(PPh3)4 (1.04 g, 0.873 mmol) and a soln. of Na2CO3 (7.38 g, 69.6 mmol) in 35 ml H2O is added. The reaction mixture is stirred at 90° C. for 15 h. After cooling to rt the mixture is filtered over hyflo, the filtrate is extracted with water and brine. The aq. layers are reextracted with AcOEt and the combined organic layers are dried over Na2SO4, filtered and the filtrate is evaporated. The resulting crude product is purified by FC (255 g silica gel, eluent AcOEt/MeOH/Et3N 70:27:3) and recrystallization from EtOH to give 3.87 g (67%) (4S,5R)-4-[5-(1H-indol-5-yl)-pyrimidin-2-yloxy]-1-aza-bicyclo[3.3.1]nonane. MS (ES+): m/e=335 (MR+), m.p. 195-199° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637517B2
Source datasetuspto-grants-2014_01
ORD IDord-e5f96f413ea24b4c81a728c70058342e
Source noteuspto-grants-2014_01