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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 19637Erstellt: 23. Oktober 2026

Triethylamine → N-(4-(Trifluoromethyl)phenyl)-5,6,7,8-tetrahydro-6-phenylpyrido[4,3-d]pyrimidin-4-amine

https://huagongshe.com/de/reaction/19637

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktPhenylboronic AcidHCID 66827—
Edukt(5,6,7,8-Tetrahydro-pyrido[4,3-d]pyrimidin-4-yl)-(4-trifluoromethylphenyl)amineHCID 59346476—
KatalysatorCupric acetateHCID 8895—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-(4-(Trifluoromethyl)phenyl)-5,6,7,8-tetrahydro-6-phenylpyrido[4,3-d]pyrimidin-4-amineHCID 593464586,4%

Reaktionsschritte

The (5,6,7,8-Tetrahydro-pyrido[4,3-d]pyrimidin-4-yl)-(4-trifluoromethylphenyl)amine (100 mg, 0.34 mmol) was dissolved in anhydrous THF (2 mL). To the mixture was added phenylboronic acid (83 mg, 0.68 mmol), Cu(OAc)2 (124 mg, 0.68 mmol) and triethylamine (0.68 g, 0.095 mL). The mixture was agitated for 6 h and the solvent was removed under the vacuum. The residue was purified using a gradient of ethyl acetate:hexane (0-100%) to give the desired compound as reddish powder (8.0 mg, 6.0%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745451B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-c5c8838fa6d540bc9becc3ac0dc4c426
Quellennotizuspto-grants-2010_06