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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858289Generated: November 1, 2026

Aniline → HCID 22125037, compound

https://huagongshe.com/reaction/1858289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantHCID 22124977HCID 22124977—
ProductHCID 22125037HCID 2212503767%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 160 mg (0.3 mmol) of 3-(2-bromophenyl)-3,4-dihydro-7-methanesulfonyl-1-(1-naphthyl)pyrimido[4,5-d]pyrimidin-2(1H)-one and 200 μl (2.2 mmol) of aniline was heated at 120° C. for 2 hours. The residue was partitioned between ethyl acetate (10 ml) and 2M hydrochloric acid (10 ml) and the ethyl acetate layer separated then washed with saturated aqueous sodium bicarbonate (10 ml), dried over magnesium sulfate, filtered and evaporated to give 100 mg (67%) of 7-anilino-3-(2-bromophenyl)-3,4-dihydro-1-(1-naphthyl)pyrimido[4,5-d]pyrimidin-2(1H)-one as an orange solid of melting point 120-125° C. [Mass spectrum (ESI) MH+ =522].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06150373
Source datasetuspto-grants-2000_11
ORD IDord-f1543f38c79f4777b1f25d5b26fae83b
Source noteuspto-grants-2000_11