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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881669Generated: November 2, 2026

Benzylamine → HCID 68937709, compound

https://huagongshe.com/reaction/1881669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
ReactantTriethylamineHCID 8471—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant6-Iodoquinazolin-4-oneHCID 135401666—
SolventTolueneHCID 1140—
SolventMethyl Isobutyl KetoneHCID 7909—
ProductHCID 68937709HCID 6893770994.8%

Reaction Steps

In a 20 ml-volume glass vessel equipped with a stirrer, a thermometer and a reflux condenser were placed 2.0 g (7.4 mmol) of 6-iodoquinazolin-4-one) 1.35 g (8.8 mmol) of phosphorus oxychloride, and 10 mL of toluene in a nitrogen atmosphere. While the mixture was stirred at room temperature, 0.66 g (6.6 mmol) of triethylamine was slowly added. The resulting mixture was heated to 75° C., and then reaction was carried out for 2 hours. Subsequently, the mixture was cooled to room temperature, and 3 mL of methyl isobutyl ketone and 3.15 g (29.4 mmol) of benzylamine were added. The resulting mixture was again heated to 75° C., and then reaction was carried out under stirring for one hour. After the reaction was complete, the reaction mixture was cooled to room temperature. Thus precipitated crystalline product was collected by filtration. Subsequently, the crystalline product was placed in 30 mL of aqueous sodium hydroxide (1 mol/L), and the aqueous mixture was stirred for 30 minutes at room temperature. The crystalline product was collected by filtration, washed with 30 mL of water, and dried under reduced pressure, to give 2.26 g (isolated yield: 84%, purity 99% in terms of area percentage determined by high performance liquid chromatography) of 6-iodo-4-benzyl-aminoquinazoline as a yellowish crystalline product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318932B2
Source datasetuspto-grants-2012_11
ORD IDord-dd27f7d6cdc544c18f6a56d6dd4f01cb
Source noteuspto-grants-2012_11