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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 76429Erstellt: 23. Oktober 2026

2,4-Dichloro-5-fluoropyrimidine → 2-chloro-5-fluoro-N4-(1,2,3,4-tetrahydro-1-oxonaphthalen-7-yl)-4-pyrimidineamine

https://huagongshe.com/de/reaction/76429

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,4-Dichloro-5-fluoropyrimidineHCID 250705—
Edukt7-Amino-1,2,3,4-tetrahydronaphthalen-1-oneHCID 327177—
Produkt2-chloro-5-fluoro-N4-(1,2,3,4-tetrahydro-1-oxonaphthalen-7-yl)-4-pyrimidineamineHCID 22060787—

Reaktionsschritte

In a like manner to the preparation of 2-chloro-N4-(3,4-ethylenedioxyphenyl)-5-fluoro-4-pyrimidineamine, 2,4-dichloro-5-fluoropyrimidine and 7-amino-1-tetralone were reacted to provide 2-chloro-5-fluoro-N4-(1,2,3,4-tetrahydro-1-oxonaphthalen-7-yl)-4-pyrimidineamine. 1H NMR (DMSO-d6): δ 10.08 (s, 1H), 8.31 (d, 1H, J=3.3 Hz), 8.15 (d, 1H, J=2.4 Hz), 7.82 (dd, 1H, J=2.4 and 8.1 Hz), 7.36 (d, 1H, J=8.1 Hz), 2.91 (t, 2H, J=6.0 Hz), 2.59 (t, 2H, J=6.0 Hz), 2.07-1.98 (m, 2H); LCMS: purity: 93%; MS (m/e): 294 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08835430B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-b6930783b4724fbcaafb315e127df037
Quellennotizuspto-grants-2014_09