Triethylamine → 6-Bromo-4-chloro-9-(2-trimethylsilanyl-ethoxymethyl)-9H-dipyrido[2,3-b;4',3'-d]pyrrole

HRID 60317Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 60317
[Br:1][C:2]1[N+:10]([O-])=[CH:9][C:8]2[N:7]([CH2:12][O:13][CH2:14][CH2:15][Si:16]([CH3:19])([CH3:18])[CH3:17])[C:6]3[N:20]=[CH:21][CH:22]=[C:23]([Cl:24])[C:5]=3[C:4]=2[CH:3]=1.BrC1[N+]([O-])=CC2N(COCC[Si](C)(C)C)C3N=C(Cl)C=CC=3C=2C=1.C(N(CC)CC)C>C(#N)C>[Br:1][C:2]1[N:10]=[CH:9][C:8]2[N:7]([CH2:12][O:13][CH2:14][CH2:15][Si:16]([CH3:17])([CH3:18])[CH3:19])[C:6]3[N:20]=[CH:21][CH:22]=[C:23]([Cl:24])[C:5]=3[C:4]=2[CH:3]=1

Komponenten

5

Versuchsvorschrift

A solution of 6-bromo-4-chloro-9-(2-trimethylsilanyl-ethoxymethyl)-9H-dipyrido[2,3-b;4′,3′-d]pyrrole-7-oxide with 6-bromo-2-chloro-9-(2-trimethylsilanyl-ethoxymethyl)-9H-dipyrido[2,3-b;4′,3′-d]pyrrole-7-oxide (4:1, 90 mg, 0.2 mmol), 1,1′-[bis(diphenylphosphino)ferrocene]dichloropalladium(II) (8.5 mg, 0.012 mmol), and triethylamine (0.1 mL, 0.7 mmol) in acetonitrile (1.2 mL) was heated under microwave irradiation at 130° C. for 10 minutes. The cooled reaction mixture was concentrated in vacuo and purified by flash chromatography (silica, 40 g, ISCO, 0-40% ethyl acetate in heptane) to afford the title compound as a 4:1 mixture of the title compound with 6-bromo-2-chloro-9-(2-trimethylsilanyl-ethoxymethyl)-9H-dipyrido[2,3-b;4′,3′-d]pyrrole as an off-white solid (60 mg, 70%). The mixture was used in subsequent steps without any further purification.

Aufarbeitung

  1. customThe cooled reaction mixture
  2. concentrationwas concentrated in vacuo
  3. custompurified by flash chromatography (silica, 40 g, ISCO, 0-40% ethyl acetate in heptane)

Quellen und Nachweise

ORD-Eintrag
ord-39bba96841384a5f995f41a1a87ff984
Quelldatensatz
uspto-grants-2016_09
Patentnummer
US09440976B2

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