HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440225Generated: November 1, 2026
Sodium Bicarbonate → (R)-3-(N-benzyloxycarbonylpyrrolidin-2-ylmethyl)-5-dibenzylamino-1H-indole
https://huagongshe.com/reaction/1440225
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | (R)-3-(N-benzyloxycarbonylpyrrolidin-2-ylcarbonyl)-5-dibenzylamino-1H-indole | HCID 10414998 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (R)-3-(N-benzyloxycarbonylpyrrolidin-2-ylmethyl)-5-dibenzylamino-1H-indole | HCID 9984453 | 70% |
Reaction Steps
To a stirred solution of (R)-3-(N-benzyloxycarbonylpyrrolidin-2-ylcarbonyl)-5-dibenzylamino-1H-indole (1.50 g, 2.75 mmol) in anhydrous tetrahydrofuran (30 mL) was added lithium borohydride (0.24 g, 11.0 mmol, 4.0 eq) as a solid. The resulting reaction mixture was heated at reflux for 4 hours. A saturated solution of sodium hydrogen carbonate (10 mL) was then added, and this mixture was stirred at room temperature for 30 minutes. This aqueous mixture was then extracted with ethyl acetate (3×25 mL), and the organic extracts were combined, dried (MgSO4), and evaporated under reduced pressure. Column chromatography of the residue using silica gel (approximately 50 g) and elution with ethyl acetate/hexanes [1:3] afforded the title compound (1.02 g, 70%) as a white foam: FAB LRMS (m/z, relative intensity) 530 (MH+, 87), 529 (M+, 100), 439 (10), 409 (10), 325 (32), 235 (20).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05498626 |
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| Source dataset | uspto-grants-1996_03 |
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| ORD ID | ord-11c6678a80f746ab9e2ca8dcdfba28fd |
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| Source note | uspto-grants-1996_03 |
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