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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735349Generated: October 31, 2026

Methylamine → 4-Amino-2-methylamino-6-(2-chlorophenyl)-5,6,7,8-tetrahydroquinazoline

https://huagongshe.com/reaction/1735349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant4-Amino-2-methylsulfinyl-6-(2-chlorophenyl)-5,6,7,8-tetrahydroquinazolineHCID 19705262—
SolventEthanolHCID 702—
Product4-Amino-2-methylamino-6-(2-chlorophenyl)-5,6,7,8-tetrahydroquinazolineHCID 19705193—

Reaction Conditions

Temperature180 °C

Reaction Steps

A suspension of 1.6 grams (0.005 mole) of 4-amino-2-methylsulfinyl-6-(2-chlorophenyl)-5,6,7,8-tetrahydroquinazoline (prepared as in Example 17) and 10 mL of aqueous 40% methylamine in 50 mL of ethanol is placed in a glass tube, which is then sealed. The sealed tube is heated at about 180° C. for 7 hours and then is cooled in an ice-bath and opened. The reaction mixture is concentrated under reduced pressure to a residue. The residue is stirred with an aqueous 10% potassium carbonate solution, and the resultant suspension is extracted with chloroform. The extract is dried with magnesium sulfate and filtered. The filtrate is concentrated under reduced pressure to a residue. The residue is subjected to column chromatography on silica gel, yielding 4-amino-2-methylamino-6-(2-chlorophenyl)-5,6,7,8-tetrahydroquinazoline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05536725
Source datasetuspto-grants-1996_07
ORD IDord-1b549385057849679535cb4390a649c5
Source noteuspto-grants-1996_07