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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2252735Erstellt: 27. Oktober 2026

Citric Acid → Ethanesulfonic acid [6-[2-(5-methoxy-pyrimidin-2-yloxy)-ethoxy]-5-(2-methoxy-phenoxy)-[2,2']bipyrimidinyl-4-yl]-amide

https://huagongshe.com/reaction/2252735

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCitric AcidHCID 311—
EduktSodium hydrideHCID 24758—
Edukt2-Chloro-5-methoxypyrimidineHCID 589058—
EduktEthanesulfonic acid [6-(2-hydroxy-ethoxy)-5-(2-methoxy-phenoxy)-[2,2]bipyrimidinyl-4-yl]-amideHCID 59645268—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktEthanesulfonic acid [6-[2-(5-methoxy-pyrimidin-2-yloxy)-ethoxy]-5-(2-methoxy-phenoxy)-[2,2']bipyrimidinyl-4-yl]-amideHCID 5964526955,2%

Reaktionsbedingungen

Temperatur75 °C

Reaktionsschritte

Ethanesulfonic acid [6-(2-hydroxy-ethoxy)-5-(2-methoxy-phenoxy)-[2,2′]bipyrimidinyl-4-yl]-amide (89 mg) was dissolved in THF (6 ml). Sodium hydride (40 mg) and 2-chloro-5-methoxy-pyrimidine (92 mg) were added and the mixture was heated to 75° C. for 46 h, then poured onto water, acidified with solid citric acid and the precipitate was filtered off. The crude material was purified by crystallization from methanol to give ethanesulfonic acid [6-[2-(5-methoxy-pyrimidin-2-yloxy)-ethoxy]-5-(2-methoxy-phenoxy)-[2,2′]bipyrimidinyl-4-yl]-amide (61 mg) as a white powder. LC-MS: tR: 3.87, [M−H]+: 554.02.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07323465B2
Quelldatensatzuspto-grants-2008_01
ORD IDord-8138d20e24d94332a8035fd61bd7b0ff
Quellennotizuspto-grants-2008_01