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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1382965Erstellt: 25. Oktober 2026

o-Desmethyl metoclopramide → 4-Amino-5-chloro-N-(2-diethylamino-ethyl)-2-(1-ethyl-2-oxo-propoxy)-benzamide

https://huagongshe.com/reaction/1382965

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukto-Desmethyl metoclopramideHCID 9817332—
Edukt3-Bromo-2-pentanoneHCID 10012249—
LösungsmittelAcetonitrileHCID 6342—
Produkt4-Amino-5-chloro-N-(2-diethylamino-ethyl)-2-(1-ethyl-2-oxo-propoxy)-benzamideHCID 1411689420,3%

Reaktionsschritte

A solution of the tetrabutylammonium salt of 4-amino-5- chloro-N-[2-(diethylamino)ethyl]-2-hydroxybenzamide (10.5 g, 20 mmoles) (from Preparation No. 3) in acetonitrile (150 ml) was treated with 3-bromo-2-pentanone (3.3 g of 80%, 20 mmoles, contaminated with 15% of 1-bromo-2-pentanone) [obtained according to the procedure of E. T. Borrows, D. O. Holland and J. Kenyon, J. Chem. Soc. 1083, (1946)]. After 3 hours, the solvent was evaporated and the residue partitioned between ethyl acetate and water. The organic phase was washed with water, dried, and the solvent evaporated. The semisolid residue was triturated with ether to yield a solid which was recrystallized from etherpetroleum ether to yield 1.5 g of the title compound, mp. 75°-78°. The NMR spectrum (90 MHz) in CDCl3 gave the following resonances: δ8.26 (s, 1H); 8.14 (bs, 1H); 6.1 (s, 1H); 4.5 (t, 1H); 4.4 (s, 2H); 3.69 (q, 2H); 2.64 (m, 6 H); 2.1 (s, 3H); 2.1-1.7 (m, 2H); 1.05 (m, 9H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04808624
Quelldatensatzuspto-grants-1989_02
ORD IDord-e66f7f589b6d4e17bb90f44fa34a51a3
Quellennotizuspto-grants-1989_02