HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858288Generated: November 2, 2026
Hydrazine hydrate (1:1) → HCID 22125163, compound
https://huagongshe.com/reaction/1858288
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 22124998 | HCID 22124998 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22125163 | HCID 22125163 | 43.4% |
Reaction Steps
A solution of 160 mg (0.253 mmol) of 7-anilino-3-(2-bromophenyl)-3,4-dihydro-1-[4-(phthalimidomethyl)phenyl]pyrimido[4,5-d]pyrimidin-2(1H)-one and 0.5 ml of hydrazine hydrate in 5 ml of ethanol was stirred at room temperature under an atmosphere of nitrogen for 4 hours. The reaction mixture was evaporated and the residue purified by flash chromatography on silica gel using dichloromethane/methanol/acetic acid/water (240:24:3:2) as the eluent. Product containing fractions were combined and evaporated and the residue re-evaporated with toluene. The residue was then dissolved in 20 ml of dichloromethane, washed with saturated aqueous sodium bicarbonate (20 ml), dried over magnesium sulfate, filtered and evaporated to give 55 mg (43%) of 1-[4-(aminomethyl)phenyl]-7-anilino-3-(2-bromophenyl)-3,4-dihydropyrimido[4,5-d]pyrimidin-2(1H)-one as a white solid of melting point 133-136° C. [Mass spectrum (ESI) MH+ =501].
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-b3517f28aba2465083a920b6a9da4f2e |
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| Source note | uspto-grants-2000_11 |
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