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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855942Generated: November 1, 2026

Sodium Chloride → HCID 21106341, compound

https://huagongshe.com/reaction/855942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantMethyl iodideHCID 6328—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178508676HCID 178508676—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 21106341HCID 21106341—

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine VI, 400 mg, 1.23 mmol) in tetrahydrofuran (20 mL) at 25° C. was treated with sodium hydroxide (98 mg, 2.46 mmol), methyl iodide (0.09 mL, 1.48 mmol), and tetrabutylammonium bromide (198 mg, 0.62 mmol), and the resulting mixture stirred at 25° C. for 18 h. The reaction mixture was treated with ethyl acetate, water, and a saturated aqueous sodium chloride solution, shaken and separated. The aqueous layer was extracted with ethyl acetate, and the combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo to afford 6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine (500 mg) as a yellow solid. The product was taken on into the next reaction without further purification 6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine VIII.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262297B2
Source datasetuspto-grants-2007_08
ORD IDord-2274f6105f6c4bad8538eff3e1e70ab2
Source noteuspto-grants-2007_08