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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1042279Erstellt: 24. Oktober 2026

Lithium Hexamethyldisilazide → N5-(3-(1H-pyrazolo[3,4-d]pyrimidin-4-yl)pyridin-2-yl)-6-methyl-N1-(3-(trifluoromethyl)phenyl)isoquinoline-1,5-diamine

https://huagongshe.com/de/reaction/1042279

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktLithium HexamethyldisilazideHCID 2733832—
EduktAmmonia methanolHCID 21705897—
Edukt6-methyl-N1-(3-(trifluoromethyl)phenyl)isoquinoline-1,5-diamineHCID 44478903—
Edukt4-(2-fluoropyridin-3-yl)-1H-pyrazolo[3,4-d]pyrimidineHCID 59627383—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelMethanolHCID 887—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN5-(3-(1H-pyrazolo[3,4-d]pyrimidin-4-yl)pyridin-2-yl)-6-methyl-N1-(3-(trifluoromethyl)phenyl)isoquinoline-1,5-diamineHCID 59627374—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A mixture of 4-(2-fluoropyridin-3-yl)-1H-pyrazolo[3,4-d]pyrimidine (30 mg, 139 μmol) and 6-methyl-N1-(3-(trifluoromethyl)phenyl)isoquinoline-1,5-diamine (49 mg, 153 μmol) in THF (3 mL) was treated with lithium bis(trimethylsilyl)amide (1.0 M solution in THF; 627 μL, 627 μmol). The mixture was stirred at it for 3 h and then heated in a microwave at 100° C. for 20 min. The mixture was poured into MeOH (15 mL) and AcOH (0.5 mL) and then 2M NH3/MeOH (30 mL) was added. Solvent was removed in vacuo. The product was purified by flash chromatography eluting with MeOH/DCM (1-5%) to give N5-(3-(1H-pyrazolo[3,4-d]pyrimidin-4-yl)pyridin-2-yl)-6-methyl-N1-(3-(trifluoromethyl)phenyl)isoquinoline-1,5-diamine. MS (ESI, pos. ion) m/z: 513.2 [M+H]+

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08557830B2
Quelldatensatzuspto-grants-2013_10
ORD IDord-a42f435d804941c493cca516a3753c8a
Quellennotizuspto-grants-2013_10