HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270715Generated: October 26, 2026
3-Pyridinemethanamine → HCID 59833940, compound
https://huagongshe.com/reaction/270715
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Pyridinemethanamine | HCID 31018 | — |
| Reactant | 1,3-Bis(2,6-diisopropylphenyl)imidazolium chloride | HCID 2734913 | — |
| Reactant | HCID 59833848 | HCID 59833848 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 59833940 | HCID 59833940 | — |
Reaction Steps
N-[3-(7-Chloro-1-methyl-2-oxo-1,2-dihydro-[1,6]naphthyridin-3-yl)-4-methyl-phenyl]-3-trifluoromethyl-benzamide (50 mg, 0.106 mmol) is mixed with 3-(aminomethyl)-pyridine (18 mg, 0.16 mmol), Pd2(dba)2 (2.4 mg, 2.5%), 1,3-Bis(2,6-di-i-propylphenyl)-imidazolium chloride (2.3 mg, 5%) and potassium tert-butanoxide (17.8 mg, 0.159 mmol) under an argon environment. 6 mL of anhydrous 1,4-dioxane is added and the reaction is continued at 100° C. for 14 hours. After cooling and removal of solvent under vacuum, the crude product is dissolved in DMSO and purified by reverse phase preparative HPLC to give the final product as a pale solid: 1H NMR 400 MHz (DMSO-d6) δ 10.46 (s, 1H), 8.79 (s, 1H), 8.68 (d, 1H, J=4.6 Hz), 8.44 (s, 1H), 8.29 (s, 1H), 8.24 (t, 2H, J=7.5 Hz), 7.96 (d, 2H, J=7.8 Hz), 7.76 (m, 3H), 7.65 (m, 2H), 7.24 (d, 1H, J=8.3 Hz), 6.46 (s, 1H), 4.74 (s, 2H), 3.52 (s, 3H), 2.11 (s, 3H); MS m/z 544.3 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07449582B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-303fec6bc46e41e98819c7cf2db26445 |
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| Source note | uspto-grants-2008_11 |
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