Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Tetrahydro-4H-pyran-4-one | HCID 121599 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 57423926 | HCID 57423926 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 69122585 | HCID 69122585 | — |
Reaction Steps
1-(4-Piperidinyl)-6-[(trifluoromethyl)oxy]-1,3-dihydro-2H-benzimidazol-2-one hydrochloride D32 (0.6 g) 1,2-dichloroethane (50 mL) and triethylamine (10 mL), tetrahydro-4H-pyran-4-one (1.2 g), sodium triacetoxyborohydride (1.3 g) was stirred at room temperature over night. The mixture was poured into dilute ammonium chloride solution and extracted with dichloromethane. The organic phase was separated, washed with brine and dried with hydromatrix. The solvent was removed and the residue was chromatographed on silica gel eluted with dichloromethane/2M ammonia in methanol 0-10%. The resulting product was dissolved in a mixture of methanol and dichloromethane, treated with 1M hydrogen chloride in ether and the solvent was removed. Recrystallisation from methanol gave the title compound as a white solid (0.28 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08288413B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-2bdcc80a58d8478c9c7ebcd5f57223b6 |
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| Source note | uspto-grants-2012_10 |
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