Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 59850202 | HCID 59850202 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69128467 | HCID 69128467 | — |
Reaction Steps
A stirred suspension of 4-{4-[6-bromo-2-oxo-5-(trifluoromethyl)-2,3-dihydro-1H-benzimidazol-1-yl]-1-piperidinyl}tetrahydro-2H-pyran-4-carbonitrile (D70, 1100 mg, 0.21 mmol) in tetrahydrofuran (8 ml) at room temperature under argon was treated with 3M methylmagnesium bromide solution in diethyl ether (0.15 ml, 0.46 mmol) and the insoluble material rapidly dissolved. Further methylmagnesium bromide solution was added after a total of 50 minutes (0.15 ml) and a total of 70 minutes (0.20 ml). After another 15 minutes the reaction mixture was cooled to 0° C. and treated dropwise with 1M aq. NH4Cl solution (3 ml), then diluted with water (15 ml) and extracted with ethyl acetate. The extract was washed with brine, dried (Na2SO4) and concentrated under vacuum to afford the title compound as a white solid. This was converted to its HCl salt as a white solid (95 mg, 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08288412B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-25331d61deaf45d19cc0d475a8109b1c |
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| Source note | uspto-grants-2012_10 |
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