Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 46836198 | HCID 46836198 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 46836601 | HCID 46836601 | — |
Reaction Steps
150 mg (0.22 mmol) of 3-(6-oxo-1-{3-[5-(piperidin-4-ylmethoxy)pyrimidin-2-yl]benzyl}-1,6-dihydropyridazin-3-yl)benzonitrile is suspended in 5 ml of acetone, and 94 mg (0.45 mmol) of sodium triacetoxyborohydride are added. 200 μl of acetic acid are added to the reaction mixture, which is then stirred at 40° C. for 15 h. A further 94 mg (0.45 mmol) of sodium triacetoxyborohydride are subsequently added, and the mixture is stirred at 40° C. for 24 h. The reaction mixture is filtered, and the residue is washed with THF. The filtrate is stripped off to dryness and purified by means of preparative HPLC.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08637518B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-106bc06e392941ada8a8638886926c66 |
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| Source note | uspto-grants-2014_01 |
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