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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2052664Generated: October 30, 2026

2-Aminopyrimidine → HCID 20544711, compound

https://huagongshe.com/reaction/2052664

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminopyrimidineHCID 7978—
ReactantHCID 20544693HCID 20544693—
SolventMethyl Ethyl KetoneHCID 6569—
ProductHCID 20544711HCID 20544711—

Reaction Conditions

Temperature10 °C

Reaction Steps

280 ml of methyl ethyl ketone, 13 g of 2-amino-pyrimidine were put into a 500 ml balloon flask provided with a stirrer and a thermometer. The mixture was cooled to 10° C. and 28 g of ground 6-chloro-1,4-benzodioxane-5-carbonyl chloride was added and stirred for two hours, the temperature being allowed to rise to 20° C. The obtained solid was filtered off, washed with 30 ml of methyl ethyl ketone and then dissolved in 250 ml of boiling water. The solution was treated with 10 ml of 36° Bel caustic soda lye. After filtration 12 g of product were obtained and crystallized again from 150 ml of ethanol. 9.5 g of N-(2-pyrimidyl)-6-chloro-1,4-benzodioxane-5-carboxamide was obtained. (M.P.: 223° C. with decomposition). The structure was confirmed by nuclear magnetic resonance analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04186135
Source datasetuspto-grants-1980_01
ORD IDord-a5f10db2228c4c4bbaf966111bacacda
Source noteuspto-grants-1980_01