HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619712Generated: November 2, 2026
Ammonium formate → N-(2,4-Dimethoxybenzyl)pyrimidin-4-amine
https://huagongshe.com/reaction/1619712
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | HCID 55190931 | HCID 55190931 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(2,4-Dimethoxybenzyl)pyrimidin-4-amine | HCID 63362995 | 97% |
Reaction Steps
6-Chloro-N-(2,4-dimethoxybenzyl)pyrimidin-4-amine (Preparation 112, 3.46 g, 12.39 mmol) was dissolved in ethanol (140 mL). The solution was degassed and then 10% palladium on carbon (0.98 g) was added followed by ammonium formate (4.55 g, 72.15 mmol) and the reaction was heated at 80° C. for 2 hours. The reaction was cooled to room temperature, filtered through pad of Celite™ and the filtrate was concentrated in vacuo. The residue was partitioned between dichloromethane (30 mL) and water (15 mL). The organic layer was separated, dried over anhydrous MgSO4, filtered and evaporated to give the title compound (2.94 g, 97%) as viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08772293B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-f5c571e401594ebf840393c41adefd7e |
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| Source note | uspto-grants-2014_07 |
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