HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226141Generated: October 31, 2026
3-Pyridinemethanamine → HCID 67019582, compound
https://huagongshe.com/reaction/226141
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Pyridinemethanamine | HCID 31018 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-(3-Chlorosulfonylphenyl)acrylic acid methyl ester | HCID 73708742 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 67019582 | HCID 67019582 | 71.2% |
Reaction Steps
A solution of 3-(3-chlorosulfonylphenyl)acrylic acid methyl ester (3) (0.40 g, 1.53 mmol) in dioxane (5 ml) was added to a mixture of 3-(aminomethyl)pyridine (0.16 g, 1.48 mmol) in dioxane (1 ml) and NaHCO3 (0.37 g, 4.49 mmol) in water (3 ml), and the resultant solution was stirred at room temperature until the completion of the reaction (control by TLC). The reaction mixture was evaporated and the residue was partitioned between ethyl acetate and water. The organic layer was washed successively with water, saturated NaCl, and dried (Na2SO4). The solvent was removed and the residue was chromatographed on silica gel with dichloromethane-methanol (20:1, v/v) as eluent. The obtained product was washed with diethyl ether to give the title compound (0.35 g, 71%) as a white solid. 1H NMR (DMSO-d6, HMDSO), δ: 3.76 (3H, s); 4.09 (2H, d, J=6.0 Hz); 6.72 (1H, d, J=16.2 Hz); 7.29 (1H, dd, J=8.0 and 5.0 Hz); 7.51-8.12 (6H, m); 8.27 (1H, br t, J=6.0 Hz); 8.31-8.50 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07557140B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-c1ba2ec4fe1f44f0bc71b27a23ff7054 |
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| Source note | uspto-grants-2009_07 |
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