Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 86702282 | HCID 86702282 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 56640794 | HCID 56640794 | 79% |
Reaction Steps
To 4-[({(2S)-5-[(benzyloxy)imino]piperidin-2-yl}carbonyl)amino]piperidine-1-carboxylic acid benzyl ester (0.4641 g, 1.00 mmol), tetrahydrofuran (3.2 ml) and acetonitrile (0.8 ml) were added, and the obtained mixture was cooled down to −10° C. Sulfuric acid (0.588 g, 6.00 mmol) and subsequently sodium borohydride (0.113 g, 3.00 mmol) were added to the mixture, and after 21 hours of stirring, saturated sodium hydrogen carbonate aqueous solution (5 ml) was added. The reaction mixture was extracted with ethyl acetate (10 ml), and the extracted mixture was analyzed with high performance liquid chromatography to find that the extracted mixture contained 0.366 g of the title compound, and the reduction reaction proceeded with yield of 79%. The diastereo selectivity was (2S,5R)/(2S,5S)=87.3/12.7 (74.6% de).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096523B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-01c53b20697f4d32b4ba8133e8122212 |
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| Source note | uspto-grants-2015_08 |
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