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HRID 30497Erstellt: 23. Oktober 2026

Ammonium Chloride → (+)-N,N-diethyl-4-[{[(S)-(4-methylphenyl)sulfinyl]amino}(8-quinolinyl)methyl]-benzamide

https://huagongshe.com/de/reaction/30497

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
EduktN,N-diethyl-4-iodobenzamideHCID 875218—
Edukt(NE,S)-4-methyl-N-(quinolin-8-ylmethylidene)benzenesulfinamideHCID 87713000—
EduktButyllithiumHCID 178418339—
LösungsmittelTolueneHCID 1140—
LösungsmittelTetrahydrofuran tolueneHCID 22635083—
Produkt(+)-N,N-diethyl-4-[{[(S)-(4-methylphenyl)sulfinyl]amino}(8-quinolinyl)methyl]-benzamideHCID 6914383023,1%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

N,N-diethyl 4-iodo-benzamide (3.1 g, 10 mmol) was dissolved in dry toluene/THF (9:1, 200 mL) and cooled to −78° C. under nitrogen. n-BuLi (7.8 mL, 1.3 M in hexane, 10 mmol) was added dropwise during 5 to 10 min. After further 5 min, 3 (1.0 g, 3.4 mmol) was added dissolved in toluene (1 mL). The solution was stirred 10 min, then NH4Cl (aq.) was added. Concentration, aqueous workup and chromatography on silica gave a total of 0.70 g (44%) of a 70:30 mixture of diastereomers. The pure major isomer 5 (0.37 g) was obtained by one more chromatography. 1H NMR (CDCl3): δ1.2 (m, 6H), 2.4 (s, 3H), 3.4 (m, 4H), 6.35 (d, J=7.5 Hz, 1 H), 6.61 (d, J=7.5 Hz,1 H), 7.15-7.55 (m, 11H), 7.75 (m, 1H), 8.12 (m, 1H), 8.75 (m, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07423154B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-6e3ffd5e9a7547cc853c664e0f6bfd9f
Quellennotizuspto-grants-2008_09