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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 4-Amino-2-methylsulfinyl-6-(2-chlorophenyl)-5,6,7,8-tetrahydroquinazoline | HCID 19705262 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Amino-2-methylamino-6-(2-chlorophenyl)-5,6,7,8-tetrahydroquinazoline | HCID 19705193 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05536725 |
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| Source dataset | uspto-grants-1996_07 |
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| ORD ID | ord-1b549385057849679535cb4390a649c5 |
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| Source note | uspto-grants-1996_07 |
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