Reaktion #171561

Reaktionsgleichung

6-bromopyridine-3-carbaldehyde

n-BuLi

7-chlorothieno[3,2-b]pyridine

→

title compound 136

Ausbeute 76.0%

6-(7-Chlorothieno[3,2-b]pyridin-2-yl)nicotinaldehyde

Ausbeute 76.0%

Lösungsmittel

THF

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.STIRRINGThe dark mixture was stirred for 10 min
2. 2
   TemperaturThe mixture was heated
3. 3
   Temperaturto reflux
4. 4
   Sonstigea precipitate formed rapidly
5. 5
   workup.WAITAfter 3 h
6. 6
   Temperaturthe reaction mixture was cooled down to r.t.
7. 7
   Sonstigequenched with 2 mL NH4Cl
8. 8
   workup.WAITleft overnight
9. 9
   SonstigeThe solid was isolated by suction filtration
10. 10
    Waschenrinsed with small amount of THF
11. 11
    workup.ADDITIONsuspended in a mixture of water (200 mL) and EtOAc (100 mL)
12. 12
    Sonstigeisolated by suction filtration
13. 13
    Sonstigefinally triturated with acetic acid (100 mL)
14. 14
    Sonstigedried in vacuum

Vorschrift

A solution of 7-chlorothieno[3,2-b]pyridine (1) (4.02 g, 23.70 mmol) in THF (150 mL) [Klemm, L. H.; Louris, J. N.; Boisvert, W.; Higgins, C.; Muchiri, D. R.; J. Heterocyclic Chem., 22, 1985, 1249-1252] was cooled to −40° C. in an acetonitrile/dry ice bath. n-BuLi (9.95 mL, 24.88 mmol, 2.5M in hexanes) was added by syringe, dropwise. The dark mixture was stirred for 15 min. Zinc chloride (24.88 mL, 24.88 mmol, 1M in ether) was added by syringe. The mixture was warmed to 0° C. then tetrakistriphenylphosphine palladium (1.095 g, 0.948 mmol) was added. The dark mixture was stirred for 10 min and 6-bromopyridine-3-carbaldehyde (4.41 g, 23.70 mmol) was added. The mixture was heated to reflux and a precipitate formed rapidly. After 3 h, the reaction mixture was cooled down to r.t., quenched with 2 mL NH4Cl and left overnight. The solid was isolated by suction filtration, rinsed with small amount of THF and suspended in a mixture of water (200 mL) and EtOAc (100 mL), isolated by suction filtration and finally triturated with acetic acid (100 mL) and dried in vacuum to afford title compound 136 (4.95 g, 76% yield). 1H NMR (400 MHz, DMSO-d6) δ (ppm): 10.13 (s, 1H), 9.14 (d, J=1.4 Hz, 1H), 8.70 (d, J=5.1 Hz, 1H), 8.65 (s, 1H), 8.53 (d, J=8.4 Hz, 1H), 8.39 (dd, J=8.4, 2.1 Hz, 1H), 7.65 (d, J=4.9 Hz, 1H). MS (m/z): 275.1 (M+H).

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