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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 742971Generated: October 26, 2026

Diisopropylethylamine → 3-methyl-6-[4-(tetrahydropyran-2-yloxy)butyl]-5,6,7,8-tetrahydro-1H-pyrido[4,3-d]pyrimidine-2,4-dione

https://huagongshe.com/reaction/742971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantLithium BromideHCID 82050—
Reactant2H-Pyran, 2-(4-chlorobutoxy)tetrahydro-HCID 170488—
Reactant3-methyl-5,6,7,8-tetrahydro-1H-pyrido[4,3-d]pyrimidine-2,4-dioneHCID 10241423—
SolventDimethylformamideHCID 6228—
Product3-methyl-6-[4-(tetrahydropyran-2-yloxy)butyl]-5,6,7,8-tetrahydro-1H-pyrido[4,3-d]pyrimidine-2,4-dioneHCID 1942332951%

Reaction Steps

27 g of ethyldiisopropylamine, 18 g of lithium bromide and 46 g of 2-(4-chlorobutoxy) tetrahydropyran (86.3% pure according to GC) were added to 36.3 g of 3-methyl-5,6,7,8-tetrahydro-1H-pyrido[4,3-d]pyrimidine-2,4-dione in 1 l of dimethylformamide, with stirring, and the mixture was stirred for 5 h at 70° C. It was concentrated under reduced pressure and 34.5 g of crude 3-methyl-6-[4-(tetrahydropyran-2-yloxy)butyl]-5,6,7,8-tetrahydro-1H-pyrido[4,3-d]pyrimidine-2,4-dione were obtained after working-up of the residue by extraction with dichloromethane and water and after drying and concentration of the combined dichloromethane phases, and this crude product was purified by column chromatography on aluminum oxide (actiVity grade III) and elution with dichloromethane/ethanol (volume ratio 90:10).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05556854
Source datasetuspto-grants-1996_09
ORD IDord-7b2a6b2f8d0b47d7a07af6a44b1a050d
Source noteuspto-grants-1996_09