HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364136Generated: October 30, 2026
4-Pyridinemethanamine → HCID 58882895, compound
https://huagongshe.com/reaction/2364136
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Pyridinemethanamine | HCID 77317 | — |
| Reactant | HCID 58882900 | HCID 58882900 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 58882895 | HCID 58882895 | — |
Reaction Steps
A mixture of ethyl 7-benzyl-4-hydroxy-1-[4-(methylsulfonyl)benzyl]-2-oxo-1,2-dihydro-1,5-naphthyridine-3-carboxylate (40 mg, 0.080 mmol) and 4-(aminomethyl)pyridine (122 μL, 1.2 mmol) in EtOH (1 mL) was heated at 120° C. in a sealed tube in a microwave for 30 min. The reaction mixture was concentrated at reduced pressure, reconstituted in CH2Cl2 and washed with a mixture of 1N HCl and brine. Drying and evaporation of the organic phase gave the product as a pale green solid: 1H NMR (CDCl3) δ 10.81 (1H, br t, J=6 Hz), 8.69 (2H, d, J=7 Hz), 8.65 (1H, d, J=1 Hz), 7.83 (2H, d, J=8 Hz), 7.76 (2H, d, J=6 Hz), 7.31 (3H, m), 7.19 (2H, d, J=8 Hz), 7.11 (1H, s), 7.03 (2H, m), 5.43 (2H, br s), 4.86 (2H, d, J=6 Hz), 4.08 (2H, s), 3.03 (3H, s); HRMS calcd for C30H26N4O5S+H+: 555.1702. Found: 555.1699.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08691991B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-a9545714a42f420783a583d4ae40cfac |
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| Source note | uspto-grants-2014_04 |
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