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HRID 1098161Erstellt: 26. Oktober 2026

2-(Trifluoromethyl)phenylhydrazine → HCID 57504514, Verbindung

https://huagongshe.com/reaction/1098161

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-(Trifluoromethyl)phenylhydrazineHCID 520800—
Edukt2-tert-butylimino-N,N-diethyl-1-methyl-1,3,2lambda5-diazaphosphinan-2-amineHCID 19990018—
Edukt4,6-Diphenoxypyrimidine-5-carbaldehydeHCID 57438655—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 57504514HCID 5750451442,7%

Reaktionsschritte

(2-(trifluoromethyl)phenyl)hydrazine (CAS no. 365-34-4) (102 mg, 0.58 mmol) was added to 4,6-diphenoxypyrimidine-5-carbaldehyde (Intermediate Z2) (169 mg, 0.58 mmol) in THF (2 mL) the resulting solution was stirred at room temperature for 5 minutes. 2-tert-butylimino-2-diethylamino-1,3-dimethyl-perhydro-1,3,2-diazaphosphorine on polystyrene (526 mg, 1.16 mmol) was added and sealed into a microwave tube. The reaction was heated to 150° C. for 10 hours in a microwave reactor and cooled to RT. The reaction mixture was filtered and evaporated to dryness. The crude product was purified by flash silica chromatography, eluting with 10 to 80% ethyl acetate in isohexane to afford the product (88 mg, 42.7%). 1H NMR (400 MHz, CDCl3) δ 7.29-7.33 (2H, m), 7.34-7.39 (1H, m), 7.49-7.58 (3H, m), 7.67-7.71 (1H, m), 7.74-7.78 (1H, m), 7.90-7.92 (1H, m), 8.08 (1H, s), 8.56 (1H, s); m/z (ES+) (M+H)+=357; HPLC tR=2.66 min.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08143263B2
Quelldatensatzuspto-grants-2012_03
ORD IDord-e1a964ae487e4f749ff07b45aea31f7a
Quellennotizuspto-grants-2012_03