HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975019Generated: October 29, 2026
Hydroxide → (R)-5-Amino-3-(N-methylpyrrolidin-2-ylmethyl)-1H-indole
https://huagongshe.com/reaction/975019
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydroxide | HCID 961 | — |
| Reactant | (R)-5-dibenzylamino-3-(N-methylpyrrolidin-2-ylmethyl)-1H-indole | HCID 10364175 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (R)-5-Amino-3-(N-methylpyrrolidin-2-ylmethyl)-1H-indole | HCID 10376533 | 99.2% |
Reaction Steps
A mixture of (R)-5-dibenzylamino-3-(N-methylpyrrolidin-2-ylmethyl) indole (1.08 g, 2.64 mmol) and palladium [II] hydroxide on carbon (0.6 g) in absolute ethanol (25 mL) was shaken under a hydrogen atmosphere (3 atm) at 40° C. for 4 hours. The resulting mixture was filtered through diatomaceous earth, and the filtrate was evaporated under pressure to afford the title compound (0.60 g, 2.62 mmol, 99%) as a white foam: 1H NMR (DMSO-d6) δ10.65 (br s, NH), 7.14 (d, J=2.2 Hz, 1H), 7.12 (d, J=8.6 Hz, 1H), 6.85 (d, J=1.6 Hz, 1H), 6.60 (dd, J=2.0 and 8.6 Hz, 1H), 3.63-2.83 (m, 7H), 2.78 (s, 3H), 2.05-1.67 (m, 4H); [α]25D =+9° (MeOH, c=1.0); HRMS: calculated for C14H19N3 : 229.1575; found 229.1593.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05607951 |
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| Source dataset | uspto-grants-1997_03 |
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| ORD ID | ord-e71217e267c546fb84da3d1ab8589595 |
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| Source note | uspto-grants-1997_03 |
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