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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408810Generated: October 31, 2026

p-Toluenesulfonic acid → HCID 86658141, compound

https://huagongshe.com/reaction/408810

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
Reactant2-ChlorobenzaldehydeHCID 6996—
ReactantHCID 58459084HCID 58459084—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 86658141HCID 8665814156.9%

Reaction Steps

Heat a mixture of 1-(5-amino-6-chloro-2-methylpyrimidin-4-ylamino)-2-methylpropan-2-ol (0.5 g, 0.002 mol), 2-chlorobenzaldehyde (0.6 g, 0.004 mol), p-toluene sulfonic acid (0.1 g) and molecular sieves (1.0 g) in toluene (25 mL) to 130° C. for 16 h. Remove the molecular sieves by filtration through diatomaceous earth, and concentrate the filtrate under reduced pressure to give a residue. Dissolve the residue in dry dichloromethane (5 mL) and add DDQ (0.47 g, 0.002 mol) at 0° C. Stir the reaction mixture at room temperature for 2 h. Dilute the reaction mixture with dichloromethane, wash with 1 N 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 methanol:dichloromethane (2:98) to give the title compound (0.4 g). ES/MS m/z 351 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759360B2
Source datasetuspto-grants-2014_06
ORD IDord-9db7123d29214c188d98c4a335cb6236
Source noteuspto-grants-2014_06