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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602386Generated: October 30, 2026

Iodine → HCID 86630620, compound

https://huagongshe.com/reaction/602386

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantIsoamyl NitriteHCID 8053—
ReactantCesium iodideHCID 24601—
Reactant2-Methylphenyl boronic acidHCID 2733267—
Reactant7-Methoxy-6-(2-methylphenyl)quinazolin-2-amineHCID 67061470—
CatalystCopper iodideHCID 83717—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 86630620HCID 86630620184.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

In a similar manner to Example 4, 2-amino-7-methoxy-6-(2-methylphenyl)quinazoline was obtained using Compound A2 and 2-methylphenylboronic acid. The obtained 2-amino-7-methoxy-6-(2-methylphenyl)quinazoline (4.38 g, 16.5 mmol) was dissolved in DME (165 mL) and the solution was added with iodine (1.05 g, 8.3 mmol), cesium iodide (4.3 g, 16.5 mmol), isoamyl nitrite (13.3 mL, 99 mmol) and copper iodide (3.1 g, 16.5 mmol), followed by stirring at 80° C. for 7 hours. After an insoluble matter was filtered off from the reaction mixture, the solvent was evaporated under reduced pressure. The residue was added with aqueous saturated sodium thiosulfate solution and 28% aqueous ammonia and the obtained crystal was collected by filtration to obtain 2-iodo-7-methoxy-6-(2-methylphenyl)quinazoline (5.76 g, 93%) as a crude product. In a similar manner to Reference Example 4 and Example 19, Compound 174 was obtained using the above-obtained 2-iodo-7-methoxy-6-(2-methylphenyl)quinazoline and 4-heptylamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906522B2
Source datasetuspto-grants-2011_03
ORD IDord-c7a31f24283c413ea8b1931dc2aaeea3
Source noteuspto-grants-2011_03