HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178874Generated: October 26, 2026
6-Methoxy-3-pyridinylamine → HCID 178471946, compound
https://huagongshe.com/reaction/2178874
Participants
| Role | Name | HCID | Charge |
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| Reactant | 6-Methoxy-3-pyridinylamine | HCID 81121 | — |
| Reactant | Butanoic acid, 2-(ethoxymethylene)-3-oxo-, ethyl ester | HCID 97734 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | HCID 178471946 | HCID 178471946 | 84.1% |
Reaction Steps
A mixture of ethyl 2-(ethoxymethylene)-3-oxobutanoate (100 g, 0.54 mol) and 2-methoxy-5-aminopyridine (67 g, 0.54 mol) in chlorobenzene (500 mL) was heated at 135° C. for 4 h in a round bottomed flask that was equipped with a distillation apparatus to collect the ethanol generated during the reaction. The reaction mixture was cooled and concentrated and the residue was triturated in diethylether and filtered to obtain the desired product (120 g, 84%) as an off-white solid: 1H NMR (500 MHz, CDCl3) δ 12.74 (d, 12.3 Hz, 1H), 8.35 (d, J=13.0 Hz, 1H), 8.07 (d, J=2.8 Hz, 1H), 7.55 (d, J=8.8, 2.9 Hz, 1H), 6.79 (d, J=8.8 Hz, 1H), 4.30 (q, J=7.1 Hz, 2H), 2.55 (s, 3H), 1.33 (t, J=7.1 Hz, 1H); ESI MS m/z 265 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09067937B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-d2f5ddbaf2fc4fda82c038c74658d278 |
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| Source note | uspto-grants-2015_06 |
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