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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815129Generated: October 30, 2026

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

https://huagongshe.com/reaction/1815129

Reaction equation

Participants

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

Reaction Steps

Substituted indolines are prepared such as by the procedures described in Scheme 21. Substituted amino-indolines 64 are prepared from the nitroindoline 62 and a ketone in the presence of NaHB(OAc)3 to form the 1-substituted indoline 63. The nitroindoline 63 is hydrogenated, such as with H2 in the presence of a catalyst, such as Pd/C, to yield the amino-indoline 64.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878714B2
Source datasetuspto-grants-2005_04
ORD IDord-4c25f06351864f12b9367d0aae766456
Source noteuspto-grants-2005_04