Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 2-Pyridinecarboxaldehyde | HCID 14273 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 11742939 | HCID 11742939 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 10283821 | HCID 10283821 | 1,883% |
Reaction Steps
The title compound 9 was prepared by dissolving compound 5 (0.45 g, 0.98 mmol) in MeOH (10 mL) with 2-pyridine carboxaldehyde (110 μL, 1.18 mmol) and HOAc (3 μL, 50 μmol). Sodium cyanoborohydride (70 mg, 1.18 mmol) was added at 0° C. and reaction stirred 48 h at 25° C. Reaction was worked up by concentration in vacuo, extraction (CH2Cl2/K2CO3(aq)) and chromatography by reverse phase HPLC to give the title compound 9,461 mg(63%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06680318B2 |
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| Source dataset | uspto-grants-2004_01 |
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| ORD ID | ord-59530886033c466b9efbbe8fe949261b |
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| Source note | uspto-grants-2004_01 |
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