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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501389Generated: November 1, 2026

Chlorosuccinimide → HCID 135829595, compound

https://huagongshe.com/reaction/501389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
Reactant7-benzyl-3,7-dihydro-6h-purin-6-oneHCID 135452693—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 135829595HCID 13582959541.5%

Reaction Steps

12.748 g of 7-benzyl-1,7-dihydropurin-6-one was dissolved in 150 ml of N,N-dimethylformamide, and 7.9 g of N-chlorosuccinimide was added thereto. The reaction solution was stirred overnight, and then diluted with ethyl acetate. The solution was washed with water and 1N hydrochloric acid, and dried over anhydrous magnesium sulfate. The solution was filtered, and the filtrate was concentrated to give 6.103 g of 7-benzyl-8-chloro-1,7-dihydropurin-6-one. This compound was combined with 20 g of t-butyl piperazine-1-carboxylate, and the mixture was heated at 150° C. After being stirred for one hour, the reaction mixture was combined with ethyl acetate and water, and partitioned. The organic layer was washed with 1N hydrochloric acid, and dried over anhydrous magnesium sulfate. After filtration, the filtrate was concentrated. The residue was purified by silica gel column chromatography. Thus, 1.539 g of the title compound was obtained from the fraction eluted with ethyl acetate-methanol (10:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772226B2
Source datasetuspto-grants-2010_08
ORD IDord-005db6546de541bb97f1781fac9d4293
Source noteuspto-grants-2010_08