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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 526153Generated: October 27, 2026

6-Methoxy-3-pyridinylamine → HCID 178471946, compound

https://huagongshe.com/reaction/526153

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Methoxy-3-pyridinylamineHCID 81121—
ReactantButanoic acid, 2-(ethoxymethylene)-3-oxo-, ethyl esterHCID 97734—
SolventChlorobenzeneHCID 7964—
ProductHCID 178471946HCID 17847194684.1%

Reaction Conditions

Temperature135 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09345709B2
Source datasetuspto-grants-2016_05
ORD IDord-dd98bd0e315e41bbbf0477496d67e4b3
Source noteuspto-grants-2016_05