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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23163Generated: October 25, 2026

Methane → 6-(4-Amino-4-methylpiperidin-1-yl)-4-(3-chloro-4-fluorophenylamino)-pyrimido[5,4-d]pyrimidine

https://huagongshe.com/reaction/23163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantHydrogen iodideHCID 24841—
ReactantHCID 178432946HCID 178432946—
SolventAcetic AcidHCID 176—
Product6-(4-Amino-4-methylpiperidin-1-yl)-4-(3-chloro-4-fluorophenylamino)-pyrimido[5,4-d]pyrimidineHCID 9952216—

Reaction Conditions

Temperature15 °C

Reaction Steps

A mixture of 80 g (0.182 mol) of (6) in 160 ml glacial acetic acid at 90° C. is added dropwise to a suspension of 11.7 g (0.378 mol) of red phosphorus in 150 ml of hydriodic acid (57%, 1.134 mol). The mixture is refluxed for 4 hours, 5 g of activated charcoal are added, the mixture is then filtered and the residue is washed with glacial acetic acid and water. The filtrate is added dropwise, with vigorous stirring, to a solution of 270 ml water, 270 ml of methanol and 270 ml of sodium hydroxide solution (50%). The mixture is stirred for a further 30 minutes at 15° C. and the solid precipitated is filtered off. This is washed twice with 500 ml of water, then suspended in 500 ml of water, filtered off and dried in vacuo at 45° C. Yield: 65.2 g (91.9%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06849734B2
Source datasetuspto-grants-2005_02
ORD IDord-08dad2180b5a4c7daee879baeb9b8b5e
Source noteuspto-grants-2005_02