HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693561Generated: November 1, 2026
4-Methoxybenzylamine → HCID 57898118, compound
https://huagongshe.com/reaction/1693561
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methoxybenzylamine | HCID 75452 | — |
| Reactant | HCID 57898026 | HCID 57898026 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 57898118 | HCID 57898118 | 80% |
Reaction Steps
To a suspension of crude 5-(4-chloro-phenyl)-6-[4-(2-chloro-pyrimidin-4-yl)-phenyl]-3-methanesulfonyl-1-phenyl-1,5-dihydro-pyrazolo[3,4-d]pyrimidin-4-one (from example 356) in EtOH (6 mL) is added 4-methoxylbenzylamine (0.4 mL). The mixture is heated at 100° C. for 24 h and then cooled down to room temperature. The precipitate is collected by filtration and washed with EtOH (2×3 mL). The solid is air dried for 14 h to provide the desired 5-(4-chloro-phenyl)-3-methanesulfonyl-6-{4-[2-(4-methoxy-benzylamino)-pyrimidin-4-yl]-phenyl}-1-phenyl-1,5-dihydro-pyrazolo[3,4-d]pyrimidin-4-one as white solid (230 mg, 80%). HPLC-MS calculated C36H28ClN7O4S (M−H′): 690.2. Found: 690.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08158634B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-29f0184b57e6421c8a279f675fbda5b3 |
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| Source note | uspto-grants-2012_04 |
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