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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093291Generated: November 3, 2026

Dimethylformamide → HCID 67456046, compound

https://huagongshe.com/reaction/2093291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Amino-4-chloro-6-methylpyrimidineHCID 21810—
Reactant(+-)-1-AminoindanHCID 123445—
ProductHCID 67456046HCID 67456046—

Reaction Conditions

Temperature145 °C

Reaction Steps

A mixture of 2.9 g (20 mmol) of 2-amino-4-chloro-6-methylpyrimidine, 2.9 g (22 mmol) of 1-aminoindane and 4.1 g (30 mmol) of potassium carbonate in 30 ml of dimethylformamide is heated at 145° C. for 3 hours. After cooling, the reaction mixture is hydrolyzed, the aqueous mixture is extracted with methylene chloride, the separated-off organic phase is dried with sodium sulfate. After filtering off the drying agent and concentrating the organic phase by evaporation, the crude mixture is separated by means of column chromatographic separation using ethyl acetate/methanol/triethylamine 90/10/1 as eluent. The 2-amino-4-indanyl-1-amino-6-methylpyrimidine obtained in this way is taken up in ethyl acetate/heptane 2:8 and treated with activated carbon. After separating off the activated carbon and concentrating the solvent by evaporation, 1 g of 2-amino-4-indanyl-1-amino-6-methylpyrimidine is obtained (glass-like solid, m.p: 53-54° C., 20% yield, 95% purity).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445408B2
Source datasetuspto-grants-2013_05
ORD IDord-dee9d0b676bb4e53bb4ca8c4f552e8f5
Source noteuspto-grants-2013_05