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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371131Generated: November 2, 2026

Sodium Carbonate → HCID 178432674, compound

https://huagongshe.com/reaction/1371131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantTriphenylphosphineHCID 11776—
ReactantMethylboronic AcidHCID 139377—
ReactantHCID 178432852HCID 178432852—
CatalystTris(dibenzylideneacetone) dipalladiumHCID 9832798—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 178432674HCID 17843267462%

Reaction Steps

A mixture of 4-chloro-2-methyl-6-phenyl-pyrrolo[3,2-d]pyrimidine (Example 1(e)) (80 mg, 0.33 mmol), methylboronic acid (Aldrich Chemical Company) (49 mg, 0.82 mmol), tris(dibenzylideneacetone) dipalladium(0) (Aldrich Chemical Company) (9.4 mg, 0.0103 mmol) and triphenylphosphine (Aldrich Chemical Company) (10.8 mg, 0.042 mmol) in a mixed solvent (1000 μL of toluene, 500 μL of 1.0 M Na2CO3, and 250 μL of ethanol) was heated at reflux under N2 overnight. Upon cooling to the room temperature, the reaction mixture was diluted with H2O (20 mL) and extracted with CHCl3 (4×40 mL). The organic extracts were dried over Na2SO4, filtered, and concentrated with a rotary evaporator. This material was purified by preparative thin layer chromatography on silica gel with 1:1 THF:hexanes as eluant to afford 30 mg (62%) of the title compound as a yellow solid. 1H NMR (CDCl3; 400 MHz): δ 8.38 (s, 1), 7.74 (d, 2, J=7.0), 7.53 (t, 2, J=7.0), 7.45 (t, 1, J=7.0), 6.87 (d, 1, J=1.7), 2.79 (s, 3), 2.74 (s, 3). MS m/z: 224 (M+1), 222 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06583154B1
Source datasetuspto-grants-2003_06
ORD IDord-f969a4266fdf49aaadeaa393bd25dcb1
Source noteuspto-grants-2003_06