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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858280Generated: October 31, 2026

Aniline → HCID 22124965, compound

https://huagongshe.com/reaction/1858280

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantHCID 54384838HCID 54384838—
SolventHydrochloric AcidHCID 313—
ProductHCID 22124965HCID 22124965100%

Reaction Conditions

Temperature180 °C

Reaction Steps

1.5 g (2 mmol) of 3-(2-bromophenyl)-1-[3-(tert-butyldiphenylsilyloxymethyl)phenyl]-3,4-dihydro-7-methanesulfonyl-pyrimido[4,5-d]pyrimidin-2(1H)-one (prepared in Example 61(h)) was treated with 3 ml of aniline and the mixture heated at 180° C. for 20 minutes and cooled. The mixture was poured into 50 ml of 2M aqueous hydrochloric acid and the precipitated product filtered off, washed with water and dried to afford 1.5 g (100%) of 7-anilino-3-(2-bromophenyl)-1-[3-((tert-butyldiphenylsilyloxy)methyl)phenyl]-3,4-dihydropyrimido[4,5-d]pyrimidin-2(1H)-one as a light brown solid. [Mass spectrum (ESI) MH+ =741].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06150373
Source datasetuspto-grants-2000_11
ORD IDord-45962892c03745d093068a33fb87d13c
Source noteuspto-grants-2000_11