Ether, ethyl ethynyl → [2-Chloro-5-((E)-2-ethoxy-vinyl)-pyrimidin-4-yl]-(2-methoxy-1,1-dimethyl-ethyl)-amine

HRID 82281

Reaktionsgleichung

Reaktionsgleichung von HRID 82281
Br[C:2]1[C:3]([NH:9][C:10]([CH3:15])([CH3:14])[CH2:11][O:12][CH3:13])=[N:4][C:5]([Cl:8])=[N:6][CH:7]=1.[B]1OC2C(=CC=CC=2)O1.[CH2:25]([O:27][C:28]#[CH:29])[CH3:26]>>[Cl:8][C:5]1[N:4]=[C:3]([NH:9][C:10]([CH3:15])([CH3:14])[CH2:11][O:12][CH3:13])[C:2](/[CH:26]=[CH:25]/[O:27][CH2:28][CH3:29])=[CH:7][N:6]=1

Komponenten

4

Versuchsvorschrift

The title compound was prepared according to the method described for Preparation 61 using (5-Bromo-2-chloro-pyrimidin-4-yl)-(2-methoxy-1,1-dimethyl-ethyl)-amine (Preparation 256), catechol borane and ethoxyacetylene (40% in hexane) to afford the title compound as light brown gum in 44% yield, 2.6 g.

Aufarbeitung

  1. customThe title compound was prepared

Quellen und Nachweise

ORD-Eintrag
ord-1ce22986ba4a440495b30bf3ade47f58
Quelldatensatz
uspto-grants-2014_09
Patentnummer
US08846698B2

Verknüpfte Notizen

Wird geladen…