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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351220Generated: November 2, 2026

Ozone → HCID 11450134, compound

https://huagongshe.com/reaction/1351220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOzoneHCID 24823—
ReactantHCID 11174663HCID 11174663—
SolventMethanolHCID 887—
ProductHCID 11450134HCID 11450134—

Reaction Steps

To a solution of (5-allyl-6,7-dimethoxy-quinazolin-4-yl)-phenyl-amine (0.35 g, 1.09 mmol) (from Example 15, Step E ,supra) in methanol (50 mL) at −78° C. was passed a continuous stream of O3 until the color of the solution became blue. The reaction solution was then purged with argon, and methyl sulfide (5 mL) (Aldrich) was added. The reaction mixture was slowly warmed to room temperature and stirred overnight. The solution was concentrated, the residue was dried in vacuo to give the desired 7,8-dimethoxy-4-phenyl-5,6-dihydro-4H-1,3,4-triaza-phenalen-5-ol as a crude yellow solid. (Yield 0.17 g, 48%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217717B2
Source datasetuspto-grants-2007_05
ORD IDord-c1ae11e5dd894b57be998ce9e35b5388
Source noteuspto-grants-2007_05