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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454314Generated: October 31, 2026

1,3-Dibromopropane → HCID 22030700, compound

https://huagongshe.com/reaction/454314

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DibromopropaneHCID 8001—
ReactantPotassium CarbonateHCID 11430—
Reactant7-hydroxy-4-(1H-indol-5-yloxy)-6-methoxyquinazolineHCID 135763116—
SolventDimethylformamideHCID 6228—
ProductHCID 22030700HCID 2203070066%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 7-hydroxy-4-(1H-indol-5-yloxy)-6-methoxyquinazoline (1 g, 3.2 mmol), (prepared as described for the starting material in Example 107), in DMF (50 ml) was added powdered potassium carbonate (1.32 g, 9.6 mmol) and 1,3-dibromopropane (6.43 g, 32 mmol). The reaction was heated at 50° C. for 2 hours. The inorganic material was filtered off and then the DMF removed. The residue was partitioned between methylene chloride/water. The organics were separated, dried over MgSO4, filtered, evaporated in vacuo and purified by flash chromatography eluting from methylene chloride to 5% methanol/95% methylene chloride. The product was concentrated in vacuo, triturated with ether and the resulting solid filtered to give 7-(3-bromopropoxy)-4-(1H-indol-5-yloxy)-6-methoxyquinazoline (900 mg, 66%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492560B2
Source datasetuspto-grants-2013_07
ORD IDord-51519725f46e4c08a2cb5c2d0fc0c720
Source noteuspto-grants-2013_07