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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1469104Generated: November 1, 2026

Sodium Bicarbonate → HCID 67513853, compound

https://huagongshe.com/reaction/1469104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 57685395HCID 57685395—
ReactantHCID 67514332HCID 67514332—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 67513853HCID 6751385356.3%

Reaction Steps

0.25 g of 4-(3,4-dihydro-2H-quinolin-1-yl)-6-iodoquinazoline, 0.30 g of 2-methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-(2-trimethylsilanylethoxymethyl)-3H-imidazo[4,5-b]pyridine, 0.16 g of sodium hydrogencarbonate and 0.09 g of Pd(PPh3)2Cl2 in 5.00 ml of dioxane and 0.50 ml of water are heated at 90° C. under nitrogen in a flask until the reaction is complete (HPLC check, about 5 hours). The cooled reaction solution is diluted with EA and washed 3 times with water. The organic phase is dried over sodium sulfate and purified by means of column chromatography (gradient EA: methanol 0-40% in 20 min), giving 0.19 g of 4-(3,4-dihydro-2H-quinolin-1-yl)-6-[2-methyl-3-(2-trimethylsilanylethoxymethyl)-3H-imidazo[4,5-b]pyridin-6-yl]quinazoline as white powder (yield 50%, content 94%); MS-FAB (M+H+)=523.2; Rf (polar method): 2.54 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006255B2
Source datasetuspto-grants-2015_04
ORD IDord-a6540d60d91f41baba02fbefe3aa9cf4
Source noteuspto-grants-2015_04