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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370062Generated: November 1, 2026

p-Toluenesulfonic acid → HCID 86675238, compound

https://huagongshe.com/reaction/2370062

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
Reactant2-ChlorobenzaldehydeHCID 6996—
ReactantHCID 86675239HCID 86675239—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 86675238HCID 866752388.9%

Reaction Steps

Heat a mixture of 2-[(5-amino-6-chloro-2-methyl-pyrimidin-4-yl)amino]acetamide (2.2 g, 0.01 mol), 2-chlorobenzaldehyde (2.86 g, 0.02 mol), p-toluene sulfonic acid (0.2 g) and molecular sieves (1.0 g) in toluene (50 mL) to reflux for 16 h. Cool and remove the sieves by filtration through diatomaceous earth. Concentrate the filtrate under reduced pressure to afford a residue. Dissolve the residue in dry dichloromethane (50 mL) and add 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (2.3 g, 0.01 mol) at 0° C. Allow to warm to room temperature and stir for 2 h. Dilute the reaction mixture with dichloromethane, wash with 1 N aqueous sodium hydroxide solution, water, and brine. Dry the organic layer over anhydrous sodium sulfate, filter, and concentrate to give a residue. Purify the residue on a silica gel column eluting with dichloromethane:methanol (98:2) to provide the title compound (0.3 g). ES/MS m/z 336 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710063B2
Source datasetuspto-grants-2014_04
ORD IDord-f7ea7c312cd44f1f909ae4f60bd6380f
Source noteuspto-grants-2014_04