Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium tetraborohydride | HCID 131720822 | — |
| Reactant | HCID 178486555 | HCID 178486555 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-Demethylivabradine | HCID 10389261 | 102.9% |
Reaction Steps
1 g of the product obtained in Step 1 (containing 47% amidine) is dissolved in 15 mL of methanol; the resulting solution is then cooled to 0° C. and 100 mg (2.61 mmol, 1.2 equivalents) of sodium tetraborohydride are added. Stirring is carried out overnight at ambient temperature, and then 5.3 mL of 20% aqueous sodium hydroxide solution and 20 mL of dichloromethane are added. Vigorous stirring is carried out for 15 minutes. The organic phase is then extracted, washed with water, dried over MgSO4, filtered and then evaporated to dryness. There is obtained 1 g of an oil which is purified by flash chromatography on 100 g of silica (eluant=dichloromethane/ethanol/NH4OH: 90/10/1) to yield 300 mg of expected product in the form of an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08101747B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-1d825601e6d547cea99d23ed41b5d6e8 |
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| Source note | uspto-grants-2012_01 |
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