Reaktion #1828218

Reaktionsgleichung

diethyl azodicarboxylate

triphenylphosphine

1-methyl-1,2,3,6-tetrahydropyridine-4-methanol

1-acetyl-6-bromo-2,3-dihydro-1H-indol-5-ol

→

1-acetyl-6-bromo-2,3-dihydro-5-(1-methyl-1,2,3,6-tetrahydropyridin-4-ylmethoxy)-1H-indole

Ausbeute 74.0%

Lösungsmittel

THF

THF

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.ADDITIONfollowed by the dropwise addition over 15 mins
2. 2
   workup.DISSOLUTIONthe insoluble material dissolved
3. 3
   Einengenconcentrated in vacuo to approx. 500 ml volume
4. 4
   SonstigeThe solid which had formed
5. 5
   Filtrationwas filtered off
6. 6
   Sonstigedried
7. 7
   EinengenThe filtrate was concentrated in vacuo
8. 8
   workup.ADDITIONthe residue treated with ethyl acetate (700 ml) and 1M HCl acid (500 ml)
9. 9
   Sonstigethe acid layer separated
10. 10
    WaschenThis was washed with ethyl acetate
11. 11
    Extraktionextracted with ethyl acetate
12. 12
    TrocknenThe combined extracts were dried (Na2SO4)
13. 13
    Einengenconcentrated in vacuo
14. 14
    Sonstigeto leave a yellow solid, which
15. 15
    Sonstigewas recrystallised from ethyl acetate (3.8 g)

Vorschrift

A stirred suspension of powdered 1-acetyl-6-bromo-2,3-dihydro-1H-indol-5-ol (Tetrahedron, 1973, 29(8), 1115) (19 g, 0.074 mole) in dry THF (1700 ml) at room temp. under argon was treated with triphenylphosphine (19.6 g, 0.075 mole) and 1-methyl-1,2,3,6-tetrahydropyridine-4-methanol (J. Med. Chem., 1988, 31, 545) (9.5 g, 0.075 mole), followed by the dropwise addition over 15 mins. of a solution of diethyl azodicarboxylate (11.8 ml, 0.075 mole) in THF (40 ml). A mild exotherm occured and the insoluble material dissolved. The solution was warmed at 32° C. for 1 hour, then concentrated in vacuo to approx. 500 ml volume. The solid which had formed was filtered off and dried according 16.1 g of beige solid. The filtrate was concentrated in vacuo and the residue treated with ethyl acetate (700 ml) and 1M HCl acid (500 ml), shaken well and the acid layer separated. This was washed with ethyl acetate, then basified with 40% NaOH and extracted with ethyl acetate, followed by chloroform. The combined extracts were dried (Na2SO4) and concentrated in vacuo to leave a yellow solid, which was recrystallised from ethyl acetate (3.8 g) giving a total yield of 19.9 g (74%) of 1-acetyl-6-bromo-2,3-dihydro-5-(1-methyl-1,2,3,6-tetrahydropyridin-4-ylmethoxy)-1H-indole.

Quelle