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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 736341Erstellt: 25. Oktober 2026

6-Bromo-N-methoxy-N-methylpicolinamide → (6-Bromo-pyridin-2-yl)-(4-chloro-7-isopropyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)-methanone

https://huagongshe.com/reaction/736341

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt6-Bromo-N-methoxy-N-methylpicolinamideHCID 24730332—
Edukt5-Bromo-4-chloro-7-isopropyl-7H-pyrrolo[2,3-d]pyrimidineHCID 45789428—
Edukt(5-Bromo-pyridin-3-yl)-(4-chloro-7-isopropyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)-methanoneHCID 86603152—
Produkt(6-Bromo-pyridin-2-yl)-(4-chloro-7-isopropyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)-methanoneHCID 8660315569%

Reaktionsschritte

The title compound (34.0 g, 69%) was prepared from 5-Bromo-4-chloro-7-isopropyl-7H-pyrrolo[2,3-d]pyrimidine (35.8 g, 130.5 mmol) and 6-Bromo-pyridine-2-carboxylic acid methoxy-methyl-amide (32.0 g, 130.5 mmol) by procedures analogous to those described for the preparation (5-Bromo-pyridin-3-yl)-(4-chloro-7-isopropyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)-methanone. MS: 380.6 (MH+); HPLC Rf: 6.05 min. (HPLC method 4); HPLC purity: 100%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07595325B2
Quelldatensatzuspto-grants-2009_09
ORD IDord-8eda0b4f3ae143f884c7a41f07949abb
Quellennotizuspto-grants-2009_09