HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858251Generated: November 2, 2026
4-(2-(Diethylamino)ethoxy)aniline → HCID 22125022, compound
https://huagongshe.com/reaction/1858251
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(2-(Diethylamino)ethoxy)aniline | HCID 418932 | — |
| Reactant | HCID 22125048 | HCID 22125048 | — |
| Solvent | Dichloromethane methanol acetic acid water | HCID 18914200 | — |
| Product | HCID 22125022 | HCID 22125022 | 11.4% |
Reaction Steps
A mixture of 200 mg (0.5 mmol) of 3-(3-bromophenyl)-7-methanesulfonyl-3,4-dihydro-1-methylpyrimido[4,5-d]pyrimidin-2(1H)-one and 300 mg (1.4 mmol) of 4-[2-(diethylamino)ethoxy]aniline was heated at 180° C. for 35 minutes and then cooled. The residue was subjected to column chromatography on silica gel using dichloromethane/methanol/acetic acid/water (240:24:3:2) for the elution. Product-containing fractions were combined, and evaporated and the residue was evaporated with toluene. The residue was then dissolved in 40 ml of dichloromethane, washed with 40 ml of saturated aqueous sodium bicarbonate solution, dried over magnesium sulfate, filtered and evaporated to give 30 mg (11%) of 3-(3-bromophenyl)-7-[4-[2-(diethylamino)ethoxy]anilino]-3,4-dihydro-1-methylpyrimido[4,5-d]pyrimidin-2(1H)-one as an off-white solid of melting point 150° 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-987f008815664e868113a3fe7122373d |
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| Source note | uspto-grants-2000_11 |
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