Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 6481592 | HCID 6481592 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 6481587 | HCID 6481587 | 68% |
Reaction Steps
LiAlH4 (0.0002 mol) was added at 5° C. to a mixture of 3-{4-[1-(3-Hydroxy-6-methyl-pyridin-2-ylmethyl)-4,6-dimethyl-1H-benzoimidazol-2-ylamino]-piperidin-1-yl}-propionic acid ethyl ester (0.00009 mol; melting point: 172° C.; prepared according to the procedure described in variant 2) in tetrahydrofuran (10 ml) under N2 flow. The mixture was stirred at 5° C. for 1 hour, then at room temperature for 3 hours. A minimum of H2O and ethylacetate were added. The organic layer was separated, dried (over MgSO4), filtered and the solvent was evaporated until dryness. The residue was crystallized from 2-propanone/CH3CN/diisopropylether. The precipitate was filtered off and dried, yielding 0.026 g of 2-{2-[1-(3-hydroxy-propyl)-piperidin-4-ylamino]-4,6-dimethyl-benzoimidazol-1-ylmethyl}-6-methyl-pyridin-3-ol (compound 4, 68%, melting point: 209° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07355051B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-e560b84bdcfe4f338d3dcec5afb715c0 |
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| Source note | uspto-grants-2008_04 |
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