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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantLithium borohydrideHCID 4148881—
Reactant(R)-3-(N-benzyloxycarbonylpyrrolidin-2-ylcarbonyl)-5-dibenzylamino-1H-indoleHCID 10414998—
SolventTetrahydrofuranHCID 8028—
Product(R)-3-(N-benzyloxycarbonylpyrrolidin-2-ylmethyl)-5-dibenzylamino-1H-indoleHCID 998445370%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05498626
Source datasetuspto-grants-1996_03
ORD IDord-11c6678a80f746ab9e2ca8dcdfba28fd
Source noteuspto-grants-1996_03