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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1058097Erstellt: 25. Oktober 2026

Ammonia → Methyl 3-amino-3-(pyridin-3-YL)prop-2-enoate

https://huagongshe.com/reaction/1058097

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
EduktFormic AcidHCID 284—
EduktIsopropanolHCID 3776—
Edukt3-Pyridinepropanoic acid, beta-oxo-, methyl esterHCID 108645—
LösungsmittelTolueneHCID 1140—
ProduktMethyl 3-amino-3-(pyridin-3-YL)prop-2-enoateHCID 69944552—

Reaktionsbedingungen

Temperatur65 °C

Reaktionsschritte

Methyl nicotinoylacetate (88 g, 0.5 mol) was dissolved in toluene (200 g), isopropyl alcohol (200 g), and formic acid (98-100%, 1.22 g, 0.03 mol) and heated to 60-65° C. Gaseous ammonia (23 g, 1.35 mol) was bubbled through the solution for 15 minutes. The white suspension was stirred at 65° C. until a homogeneous solution formed. The solution was stirred for two hours at 65° C. and then concentrated (ca. 200 g) at 65° C. The residue was cooled to −5° C. with stirring and methyl 3-amino-3-(3-pyridyl)-2-propenoate crystallized as colorless needles. The process of reducing the volume to 50% followed by cooling was repeated three times with the mother liquors. Filtration, washing with toluene, and drying at 30° C. resulted in 77.74 g (88.8%) of methyl 3-amino-3-(3-pyridyl)-2-propenoate as colorless crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06515130B1
Quelldatensatzuspto-grants-2003_02
ORD IDord-3fa5e721e718439b9d7e1fad80c683ca
Quellennotizuspto-grants-2003_02