Reaktion #4942

Reaktionsgleichung

2-(2-chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f][1,4]-oxazepine-5(4H)-thione

4-[bis(4-fluorophenyl)methyl]piperidine

ethanol

K2CO3

→

2-[2-[4-[Bis(4-fluorophenyl)methyl]-1-piperidinyl]ethyl]2,3-dihydro-4-methylpyrido[3,2-f][1,4]oxazepin-5(4H)-thione oxalate hydrate

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturat reflux for 144 hr
2. 2
   EinengenThe mixture was concentrated
3. 3
   Sonstigethe residue partitioned between chloroform and dilute sodium hydroxide
4. 4
   TrocknenThe chloroform was dried over anhydrous sodium sulfate
5. 5
   Einengenconcentrated
6. 6
   SonstigeThe residue was chromatographed on a Waters®500 HPLC
7. 7
   Wascheneluting with absolute ethanol
8. 8
   SonstigeThe material with mass 507 was collected
9. 9
   Einengenconcentrated
10. 10
    SonstigeThe residue (6 g) was reacted with 1.2 g of oxalic acid in ethanol

Vorschrift

A solution of 4 g (0.016 mole) of 2-(2-chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f][1,4]-oxazepine-5(4H)-thione and 4.5 g (0.016 mole) of 4-[bis(4-fluorophenyl)methyl]piperidine in 100 ml of ethanol was refluxed for 48 hr. One gram of K2CO3 was added and this mixture stirred at reflux for 144 hr. The mixture was concentrated and the residue partitioned between chloroform and dilute sodium hydroxide. The chloroform was dried over anhydrous sodium sulfate and concentrated. The residue was chromatographed on a Waters®500 HPLC using a silica column and eluting with absolute ethanol. The material with mass 507 was collected and concentrated. The residue (6 g) was reacted with 1.2 g of oxalic acid in ethanol. Yield was 5 g, m.p. 125°-138° C.

Quelle