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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371129Generated: October 30, 2026

Sodium Carbonate → HCID 178488971, compound

https://huagongshe.com/reaction/1371129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantTriphenylphosphineHCID 11776—
Reactant(4-Methoxyphenyl)boronic acidHCID 201262—
ReactantHCID 178432852HCID 178432852—
CatalystTris(dibenzylideneacetone) dipalladiumHCID 9832798—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 178488971HCID 17848897189%

Reaction Steps

A mixture of 4-chloro-2-methyl-6-phenylpyrrolo-[3,2-d]pyrimidine (Example 1(e)) (50 mg, 0.21 mmol), 4-methoxyphenylboronic acid (Aldrich Chemical Company) (44 mg, 0.287 mmol), tris(dibenzylideneacetone) dipalladium(0) (Aldrich Chemical Company) 4.7 mg, 0.0051 mmol, 0.025 eq) and triphenylphosphine (Aldrich Chemical Company) (10.8 mg, 0.041 mmol) in a mixed solvent (600 μL of toluene, 300 μL of 1.0 M Na2CO3, and 150 μL of ethanol) was heated at reflux under N2 for 36 h. Upon cooling to the room temperature, the reaction mixture was diluted with H2O (20 mL) and extracted with CHCl3 (3×20 mL). The organic phase was dried over Na2SO4, filtered, and concentrated with a rotary evaporator. The crude material was purified by flash chromatography on silica gel with a gradient eluant of EtOAc(0-50%):hexanes(100-50%) to afford 57 mg (89%) of the title compound as a yellow solid. Mp: 225-227° C. 1H NMR (Acetone-d6, 400 MHz): δ 10.72 (s, 1), 8.14 (d, 2, J=7.0), 8.00 (d, 2, J=8.0), 7.51 (t, 2, J=7.0), 7.44 (t, 1, J=7.0), 7.11 (d, 2, J=8.0), 6.95 (s, 1), 3.91 (s, 3), 2.70 (s, 3). MS m/z: 320 (M+1), 318 (M−1). HRMS (NBA-NaI) m/z Calcd for M++H, C20H17N3O: 316.1450. Found: 316.1450.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06583154B1
Source datasetuspto-grants-2003_06
ORD IDord-67e768febc3f4f85941ea604c4acccac
Source noteuspto-grants-2003_06