Reaktion #1130675

ord-2eacae2ddddd4258ac1e45048c35f729

Reaktionsgleichung

Cl.NNc1c(Cl)cccc1Cl
(2,6-Dichlorophenyl)hydrazine hydrochloride
CN(C)C=C1C(=O)c2cccnc2Nc2ccncc21
6-[(dimethylamino)methylene]-6,11-dihydro-5H-dipyrido[2,3-b:3′,4′-f]azepin-5-one
Clc1cccc(Cl)c1-n1cc2c(n1)-c1cccnc1Nc1ccncc1-2
desired product
Clc1cccc(Cl)c1-n1cc2c(n1)-c1cccnc1Nc1ccncc1-2
2-(2,6-Dichlorophenyl)-2,8-dihydropyrazolo[3,4-d]dipyrido[2,3-b:3′,4′-f]azepine

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe mixture was heated to 60° C. overnight
  2. 2
    TemperaturThe reaction was then cooled to room temperature
  3. 3
    Sonstigethe major product from the reaction mixture was isolated

Vorschrift

(2,6-Dichlorophenyl)hydrazine hydrochloride (168 mg, 0.788 mmol) was added to a solution of 6-[(dimethylamino)methylene]-6,11-dihydro-5H-dipyrido[2,3-b:3′,4′-f]azepin-5-one (105 mg, 0.394 mmol, Intermediate E-1) in ethanol (4 mL) and stirred at room temperature. After 30 minutes, the mixture was heated to 60° C. overnight. The reaction was then cooled to room temperature and the major product from the reaction mixture was isolated using preparative LC/MS to provide the desired product as a white powder. 1H NMR (DMSO-d6) δ 8.77 (bs, 1H), 8.45 (bs, 1H), 8.40 (bs, 1H), 8.04 (m, 2H), 7.94 (d, 1H), 7.75 (m, 2H), 7.62 (m, 1H), 6.95 (m, 1H), 6.87 (m, 1H). LC/MS: 380 (M+H)+.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08563541B2uspto-grants-2013_10