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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9731Generated: October 28, 2026

Trifluoroacetic acid → 3-(2-Bromo-phenyl)-1-methyl-7-(4-methyl-3-oxo-3,4-dihydro-2h-benzo[1,4]thiazin-7-ylamino)-3,4-dihydro-1h-pyrimido[4,5-d]pyrimidin-2-one

https://huagongshe.com/reaction/9731

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant7-Amino-4-methyl-4h-benzo[1,4]thiazin-3-oneHCID 21877770—
Reactant3-(2-bromophenyl)-7-methanesulfonyl-3,4-dihydro-1-methylpyrimido[4,5-d]pyrimidin-2(1H)-oneHCID 21988153—
SolventHydrochloric AcidHCID 313—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product3-(2-Bromo-phenyl)-1-methyl-7-(4-methyl-3-oxo-3,4-dihydro-2h-benzo[1,4]thiazin-7-ylamino)-3,4-dihydro-1h-pyrimido[4,5-d]pyrimidin-2-oneHCID 10481466—

Reaction Conditions

Temperature140 °C

Reaction Steps

320 mg 3-(2-bromo-phenyl)-3,4-dihydro-7-methanesulphonyl-1-methylpyrimido-[4,5-d]pyrimidin-2(1H)-one and 626 mg 7-amino-4-methyl-4H-benzo[1,4]thiazin-3-one (starting material k)) in 4 ml NMP were treated with 92 mg TFA and heated to 140° C. for 12 hrs. The mixture was diluted with aqueous HCl and the precipitated product collected by filtration.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091345B2
Source datasetuspto-grants-2006_08
ORD IDord-f840b6ad1baf4e27939b43cc47ae75b9
Source noteuspto-grants-2006_08