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HRID 552196Erstellt: 24. Oktober 2026

Oxdralazine dihydrochloride → 1-(2-Dimethylamino-ethyl)-5-oxo-pyrrolidine-3-carboxylic acid (6-chloro-9H-beta-carbolin-8-yl)-amide

https://huagongshe.com/de/reaction/552196

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktOxdralazine dihydrochlorideHCID 168701—
EduktAmmonium AcetateHCID 517165—
Edukt1-(2-(Dimethylamino)ethyl)-5-oxopyrrolidine-3-carboxylic acidHCID 654521—
Edukt6-Chloro-9H-beta-carbolin-8-amineHCID 21362701—
Produkt1-(2-Dimethylamino-ethyl)-5-oxo-pyrrolidine-3-carboxylic acid (6-chloro-9H-beta-carbolin-8-yl)-amideHCID 1177395370%

Reaktionsschritte

Prepared according to Method B from 6-chloro-9H-β-carboline-8-ylamine and 1-(2-dimethylamino-ethyl)-5-oxo-pyrrolidine-3-carboxylic acid in 70-80% yield as the di-HCl salt. 1H-NMR (300 MHz, D2O): δ 2.97 (dd, 1H), 3.03 (s, 6H), 3.08 (dd, 1H), 3.51 (t, 2H), 3.76-3.89 (m, 3H), 3.95 (dd, 1H), 4.01 (dd, 1H), 7.75 (d, 1H), 8.24 (d, 1H), 8.45 (dd, 1H), 8.52 (dd, 1H), 9.10 (bs, 1H). Retention Time (LC, method: ammonium acetate standard): 0.99 min. MS (M+H+): 400.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07951801B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-f65907af9bcd4ee1a0be32454d9a9347
Quellennotizuspto-grants-2011_05