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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440224Generated: November 2, 2026

(R)-3-(N-benzyloxycarbonylpyrrolidin-2-ylmethyl)-5-dibenzylamino-1H-indole → (R)-5-Amino-3-(pyrrolidin-2-ylmethyl)-1H-indole

https://huagongshe.com/reaction/1440224

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-3-(N-benzyloxycarbonylpyrrolidin-2-ylmethyl)-5-dibenzylamino-1H-indoleHCID 9984453—
CatalystPalladium hydroxideHCID 9942167—
SolventEthanolHCID 702—
Product(R)-5-Amino-3-(pyrrolidin-2-ylmethyl)-1H-indoleHCID 10262726100%

Reaction Steps

A mixture of (R)-3-(N-benzyloxycarbonylpyrrolidin-2-ylmethyl)-5-dibenzylamino-1H-indole (7.90 g, 14.91 mmol) and moist palladium (II) hydroxide on carbon (Pearlman's catalyst, 3.16 g) in absolute ethanol (100 mL) was shaken under a hydrogen atmosphere (3 atm) for 12 hours at room temperature. The resulting mixture was filtered through diatomaceous earth, and the filtrate was evaporated and dried under reduced pressure to afford the title compound as a white foam (3.20 g, 100%): 1H NMR (CD3OD) δ7.18 (d, J=8.5 Hz, 1H), 7.08 (s, 1H), 6.92 (d, J=2.0 Hz, 1H), 6.69 (dd, J=1.9 and 8.5 Hz, 1H), 3.81-3.69 (m, 1H), 3.30-2.95 (m, 4H), 2.09-1.55 (m, 4H); 13C NMR (CD3OD) δ140.1, 133.4, 129.1, 125.0, 114.6, 113.1, 109.8, 105.1, 62.1, 46.0, 31.1, 29.1, 24.3; LRMS (m/z, relative intensity) 215 (M+, 2), 198 (1) , 146 (100), 128 (7), 117 (9), 70 (60).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05498626
Source datasetuspto-grants-1996_03
ORD IDord-78dc637156c04f8f9de637274a58ddc2
Source noteuspto-grants-1996_03