HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338675Generated: October 30, 2026
Carbonic acid-guanidine (1:1) → Ethyl-3-(2-amino-7,8-dihydro-5H-pyrido[4,3-d]pyrimidin-6-yl)-benzoate
https://huagongshe.com/reaction/338675
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbonic acid-guanidine (1:1) | HCID 286947 | — |
| Reactant | Sodium Acetate Trihydrate | HCID 23665404 | — |
| Reactant | Methyl-3-(3-dimethylaminomethylene-4-oxopiperidin-1-yl)benzoate | HCID 86695813 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl-3-(2-amino-7,8-dihydro-5H-pyrido[4,3-d]pyrimidin-6-yl)-benzoate | HCID 86695814 | 49.4% |
Reaction Steps
A solution of methyl-3-(3-dimethylaminomethylene-4-oxopiperidin-1-yl)-benzoate (1.52 g, 5.27 mmol) in EtOH (100 mL) was treated with guanidine carbonate (3.80 g, 21.08 mmol), followed by addition of sodium acetate trihydrate (5.74 g, 42.16 mmol). The reaction mixture was refluxed for 15 hours and the solvent was removed in vacuo. The residue was partitioned between water and ethyl acetate and the mixture was vigorously stirred at ambient temperature for several minutes. The yellow, amorphous precipitate was collected, washed with water, ethyl acetate, and dried to give 776 mg of the title compound. The ethyl acetate layer was dried (MgSO4), filtered, and concentrated. The residue obtained was triturated with diethyl ether to give an additional 182 mg of the title compound (958 mg total, 61%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889870B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-caa3d354eeda4931a502a03b9afb6a39 |
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| Source note | uspto-grants-2014_11 |
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