HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406070Generated: October 26, 2026
2-Phenylpyrimidin-5-amine → HCID 66586937, compound
https://huagongshe.com/reaction/2406070
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Phenylpyrimidin-5-amine | HCID 786565 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 2-Nitro-5-(piperidin-1-yl)benzoic acid | HCID 14459331 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66586937 | HCID 66586937 | 12.7% |
Reaction Steps
Into a 50-mL round-bottom flask, was placed a solution of 2-nitro-5-(piperidin-1-yl)benzoic acid (1.096 g, 4.38 mmol, 1.50 equiv) in dichloromethane (20 mL), 2-phenylpyrimidin-5-amine (500 mg, 2.92 mmol, 1.00 equiv), N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (838 mg, 4.39 mmol, 1.50 equiv), and 4-dimethylaminopyridine (713 mg, 5.84 mmol, 2.00 equiv). The resulting solution was stirred overnight at 25° C. The reaction was diluted with 100 mL of water and the resulting mixture was extracted with 3×50 mL of dichloromethane. The organic layers were combined, washed with 1×100 mL of brine, dried over sodium sulfate, and concentrated under vacuum. The residue was applied onto a silica gel column and eluted with PE:EA:CH2Cl2 (20:1:0-3:1:1). The product was obtained as 150 mg (11%) of a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08809339B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-2a384607d0ac4284a2cd1c8f056eb2eb |
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| Source note | uspto-grants-2014_08 |
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