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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404656Generated: October 30, 2026

[2-(6-nitro-1H-indol-3-yl)-ethyl]-carbamic acid tert-butyl ester → [2-(6-amino-1H-indol-3-yl)-ethyl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/2404656

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[2-(6-nitro-1H-indol-3-yl)-ethyl]-carbamic acid tert-butyl esterHCID 57567411—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
Product[2-(6-amino-1H-indol-3-yl)-ethyl]-carbamic acid tert-butyl esterHCID 2107167767%

Reaction Steps

A mixture of [2-(6-nitro-1H-indol-3-yl)-ethyl]carbamic acid tert-butyl ester (5 g, 16.4 mmol) and Raney Ni (1 g) in EtOH (100 mL) was stirred at room temperature under H2 (1 atm) for 5 h. Raney Ni was filtered off and the filtrate was evaporated under reduced pressure. The crude product was purified by column chromatography to give [2-(6-amino-1H-indol-3-yl)-ethyl]-carbamic acid tert-butyl ester (B-10) (3 g, 67%). 1H NMR (DMSO-d6) δ 10.1 (br s, 1H), 7.11 (d, J=8.4 Hz, 1H), 6.77-6.73 (m, 2H), 6.46 (d, J=1.5 Hz, 1H), 6.32 (dd, J=8.4, 2.1 Hz, 1H), 4.62 (s, 2H), 3.14-3.08 (m, 2H), 2.67-2.62 (m, 2H), 1.35 (s, 9H); ESI-MS 275.8 m/z (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802700B2
Source datasetuspto-grants-2014_08
ORD IDord-b95ce688ae2f4149b3bc6ea50d70d2ed
Source noteuspto-grants-2014_08