Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Calcium Chloride | HCID 5284359 | — |
| Reactant | HCID 66714132 | HCID 66714132 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 66716120 | HCID 66716120 | 97.5% |
Reaction Steps
To a solution of 0.8 g of diethyl 4-{2-[(2-tert-butoxycarbonyl-ethyl)-(2-nitro-benzenesulfonyl)-amino]-ethoxy}-pyridine-2,6-dicarboxylate in 80 mL of ethanol were successively added 152 mg of sodium borohydride and 447 mg of CaCl2. The mixture was stirred at room temperature and 20 ml of water were then added at the end of the reaction. The ethanol was removed under reduced pressure, 100 ml of water were added to the residue obtained and the aqueous phase was extracted 3× with EtOAc. The organic phases were combined, washed with saturated NaCl solution, dried over MgSO4 and concentrated under reduced pressure. 670 mg of tert-butyl 3-[[2-(2,6-bis-hydroxymethyl-pyridin-4-yloxy)-ethyl]-(2-nitro-benzenesulfonyl)-amino]-propanoate were obtained. LC/MS (C): tr=3 min; [M+H]+: m/z 512.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09056914B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-dc9c5bbcc845410aa63ebc50e71d4905 |
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| Source note | uspto-grants-2015_06 |
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