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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1683928Generated: November 2, 2026

Hydroxide → (R)-5-Amino-3-(pyrrolidin-2-ylmethyl)-1H-indole

https://huagongshe.com/reaction/1683928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxideHCID 961—
Reactant(R)-3-(N-benzyloxycarbonylpyrrolidin-2-ylmethyl)-5-dibenzylamino-1H-indoleHCID 9984453—
CatalystPalladiumHCID 23938—
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 (ll) hydroxide on carbon (Peariman's catalyst, 3.16 g) in absolute ethanol (100 mL) was shaken under a hydrogen atmosphere (3 arm) 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 numberUS05639752
Source datasetuspto-grants-1997_06
ORD IDord-bb0614393adc472087663cc2838bac96
Source noteuspto-grants-1997_06