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HRID 1822017Erstellt: 26. Oktober 2026

Benzoyl chloride → HCID 11739497, Verbindung

https://huagongshe.com/reaction/1822017

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoyl chlorideHCID 7412—
Edukt3-((1-Methylpiperidin-4-yl)oxy)anilineHCID 39202654—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktHCID 11739497HCID 11739497—

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

Add benzoyl chloride (0.062 mL, 0.534 mmol) to a solution of 3-(1-methyl-piperidin-4-yloxy)-phenylamine (preparation 28, 102 mg, 0.494 mmol) in dioxane (3.5 mL) in a sealed tube and heat at 110° C. for 2 hr. Purification by SCX column, eluting with ammonia (2.0 N in methanol) gives the title compound as the free base (137 mg, 91%). Dissolve the residue in diethyl ether and treat with ethereal hydrogen chloride (1.0 M). Triturate the resulting gum with ether to give the title compound as the hydrochloride salt (139 mg, off-white solid). Mass spectrum (free base, ion spray): m/z=311.2 (M+1), 1H NMR (free base, CDCl3): 7.97 (bs, N—H), 7.85-7.82 (m, 2H), 7.52 (tt, J=1.3 Hz, 7.3 Hz, 1H), 7.49-7.42 (m, 3H), 7.22 (t, J=8.1 Hz, 1H), 7.05 (d, J=8.1 Hz, 1H), 6.69 (dd, J=2.1 Hz, 8.3 Hz, 1H), 4.38-4.30 (bm, 1H), 2.72-2.62 (bm, 2H), 2.35-2.23 (bm, 5H), 2.04-1.96 (bm, 2H), 1.89-1.79 (bm, 2H). Analysis calculated for C19H23ClN2O2.0.6H2O: C, 63.80; H, 6.82; N, 7.83. Found C, 63.67; H, 6.62; N, 7.83.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07608629B2
Quelldatensatzuspto-grants-2009_10
ORD IDord-ef03ae83bd2944ddae27e86e5b7682b5
Quellennotizuspto-grants-2009_10