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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351193Generated: November 4, 2026

Iodine → HCID 11385310, compound

https://huagongshe.com/reaction/1351193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantHCID 11174663HCID 11174663—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductHCID 11385310HCID 11385310—

Reaction Steps

To a solution of (5-allyl-6,7-dimethoxy-quinazolin-4-yl)-phenyl-amine (0.12 g, 0.37 mmol) (from Example 15, Step E, supra) in dichloromethane (20 mL) was added I2 (0.24 g, 1.87 mmol). The reaction mixture was stirred at room temperature for 3 hours. The mixture was diluted with chloroform (100 mL), and washed with a saturated aqueous Na2SO3 solution. The organic layer was separated, dried over Na2SO4, and concentrated. The residue was purified by chromatography using EtOAc/CH2Cl2/Et3N (1:2:0.05) as eluent to give the desired 5-iodomethyl-7,8-dimethoxy-4-phenyl-5,6-dihydro-4H-1,3,4-triaza-phenalene as a pale yellow solid. (Yield 0.11 g, 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217717B2
Source datasetuspto-grants-2007_05
ORD IDord-de55435508314d15ba5f3c4678385809
Source noteuspto-grants-2007_05