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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1462239Generated: October 29, 2026

Chloromethyl methyl sulfide → HCID 13210510, compound

https://huagongshe.com/reaction/1462239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl methyl sulfideHCID 16916—
ReactantSodium hydrideHCID 24758—
Reactant2,3-Piperazinedione, 1-(phenylmethyl)-4-((4-(2-pyrimidinylamino)phenyl)methyl)-HCID 3060247—
SolventDimethylformamideHCID 6228—
ProductHCID 13210510HCID 1321051086.45%

Reaction Steps

In 40 ml of N,N-dimethylformamide was dissolved 3.0 g of 1-benzyl-4-[4-(2-pyrimidinylamino)benzyl]-2,3-dioxopiperazine, and 0.372 g of sodium hydride (purity 52%) was added thereto, after which the resulting mixture was subjected to reaction at 80° C. for 30 min. with stirring. The reaction mixture was then cooled, and 0.72 ml of chloromethylmethylsulfide was added thereto, after which the resulting mixture was subjected to reaction at 50° to 60° C. for 2 hours. After the completion of the reaction, the reaction mixture was distilled under reduced pressure and the residue thus obtained was extracted with chloroform and then washed with water. The solution thus obtained was dried over anhydrous magnesium sulfate, and the solvent was then removed by distillation under reduced pressure. The crystals thus obtained were recrystallized from isopropyl alcohol to obtain 3.0 g (86.45% yield) of white crystalline 1-benzyl-4-{4-[N-methylthiomethyl-N-(2-pyrimidinyl)amino]benzyl}-2,3-dioxopiperazine having a melting point of 156° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04459407
Source datasetuspto-grants-1984_07
ORD IDord-d41476b81c0e4a44a2f5b2d9067aa6c3
Source noteuspto-grants-1984_07