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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 887493Generated: November 1, 2026

Nitroindoline → 2,3-dihydro-1H-indol-1-amine

https://huagongshe.com/reaction/887493

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitroindolineHCID 21959507—
CatalystPalladiumHCID 23938—
Product2,3-dihydro-1H-indol-1-amineHCID 2760932—

Reaction Steps

Substituted indolines 51 are prepared such as by the procedures described in Scheme 15. Substituted amino-indolines 48 are prepared from the nitroindoline 46 and a ketone in the presence of NaHB(OAc)3 to form the 1-substituted indoline 47. The nitroindoline 47 is hydrogenated, such as with H2 in the presence of a catalyst, such as Pd/C, to yield the amino-indoline 48.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247430B2
Source datasetuspto-grants-2012_08
ORD IDord-ae879b52ebdb44a2ac27598beae4880e
Source noteuspto-grants-2012_08