HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858217Generated: November 1, 2026
2-(4-Aminophenyl)ethylamine → HCID 22125155, compound
https://huagongshe.com/reaction/1858217
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(4-Aminophenyl)ethylamine | HCID 72895 | — |
| Reactant | 3-(2,6-dichlorophenyl)-7-methanesulfonyl-1-methyl-3,4-dihydropyrimido[4,5-d]pyrimidin-2(1H)-one | HCID 18425444 | — |
| Product | HCID 22125155 | HCID 22125155 | 3% |
Reaction Steps
A mixture of 100 mg (0.26 mmol) of 3-(2,6-dichlorophenyl)-3,4-dihydro-7-methanesulfonyl-1-methylpyrimido[4,5-d]pyrimidin-2(1H)-one and 140 mg (1 mmol) of 2-(4-aminophenyl)ethylamine was heated at 70° C. for 20 minutes. The product was purified by flash column chromatography using 5% methanol in dichloromethane for the elution. Product-containing fractions were combined and evaporated. The residue was recrystallized from ethyl acetate and 3 mg (3%) of 7-[2-(4-aminophenyl)ethylamino]-3-(2,6-dichlorophenyl)-3,4-dihydro-1-methylpyrimido[4,5-d]pyrimidin-2(1H)-one were isolated as a yellow solid of melting point 174-175° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06150373 |
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| Source dataset | uspto-grants-2000_11 |
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| ORD ID | ord-438141c0e0c44016bb81342fb9b52040 |
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| Source note | uspto-grants-2000_11 |
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