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
Participants
| Role | Name | HCID | Charge |
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| Reactant | (R)-3-(N-benzyloxycarbonylpyrrolidin-2-ylmethyl)-5-dibenzylamino-1H-indole | HCID 9984453 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (R)-5-Amino-3-(pyrrolidin-2-ylmethyl)-1H-indole | HCID 10262726 | 100% |
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
| 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-78dc637156c04f8f9de637274a58ddc2 |
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| Source note | uspto-grants-1996_03 |
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