Reaktion #534967

Reaktionsgleichung

4-Fluoro-6-methyl-1-[1-(tetrahydro-2H-pyran-4-yl)-4-piperidinyl]-1,3-dihydro-2H-benzimidazol-2-one

HCl

diethyl ether

→

4-Fluoro-6-methyl-1-[1-(tetrahydro-2H-pyran-4-yl)-4-piperidinyl]-1,3-dihydro-2H-benzimidazol-2-one hydrochloride

Lösungsmittel

methanol

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeThe solvents were evaporated
2. 2
   Sonstigethe solid triturated in diethyl ether (14.5 vol., 500 ml) for 20 min
3. 3
   SonstigeDiethyl ether was decanted
4. 4
   Sonstigethe white solid was dried under high vacuum at 40° C. overnight
5. 5
   SonstigeThe solid was dried under high vacuum overnight at 40° C
6. 6
   SonstigeThe solid was triturated in diethyl ether (14.5 vol, 500 ml)
7. 7
   Filtrationfiltered
8. 8
   Sonstigedried again in the oven at 40° C./high vacuum for 4 hours
9. 9
   workup.WAITat 60° C. overnight then at 80° C. for two hours

Vorschrift

4-Fluoro-6-methyl-1-[1-(tetrahydro-2H-pyran-4-yl)-4-piperidinyl]-1,3-dihydro-2H-benzimidazol-2-one free base (102.73 mmol, 34.25 g, 1 wt) was suspended in methanol (10 vol. 342 ml). HCl 1M in diethyl ether (154 ml, 1.5 eq.) was added dropwise in 20 min. The slurry was magnetically stirred at ambient temp. for 3 hours. The solvents were evaporated and the solid triturated in diethyl ether (14.5 vol., 500 ml) for 20 min. Diethyl ether was decanted and the white solid was dried under high vacuum at 40° C. overnight. Residual MeOH (7% w/w by NMR) was found. The solid was dried under high vacuum overnight at 40° C. The solid was triturated in diethyl ether (14.5 vol, 500 ml), filtered and dried again in the oven at 40° C./high vacuum for 4 hours, then at 60° C. overnight then at 80° C. for two hours. 36.1 g, 95%.

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