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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1729315Generated: November 3, 2026

HCID 19012102, compound → HCID 21688812, compound

https://huagongshe.com/reaction/1729315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 19012102HCID 19012102—
SolventEthanolHCID 702—
ProductHCID 21688812HCID 2168881233.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

2.0 g of the Compound v obtained in Reference Example 17 was dissolved in 20 ml of ethanol, and 4.5 g of stannic chloride (II) was added dropwise. The solution was heated up to 70° C. and then stirred for 30 minutes. The precipitated insolubles were removed by filtration, and the filtrate was then diluted with 100 ml of chloroform. Next, 20 ml of a 1N aqueous sodium hydroxide solution was added to the solution, followed by stirring vigorously. The formed insolubles were removed by filtration, and the resultant chloroform layer was separated, washed with water, dried over anhydrous sodium sulfate and then concentrated. The thus obtained oily product was purified through a silica gel column chromatograph (chloroform/methanol=100/1 in volume ratio), thereby obtaining 0.62 g of 1,3-dimethyl-6-[4-(3-[2-amino-4-methylmercaptophenoxy]propyl)piperazin-1-yl]-2,4(1H,3H)-pyrimidinedione (Compound 114).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05332739
Source datasetuspto-grants-1994_07
ORD IDord-e1fd41f564104f3d9522d4ab01e8de6d
Source noteuspto-grants-1994_07