Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238415Generated: October 31, 2026

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

https://huagongshe.com/reaction/238415

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 numberUS08642624B2
Source datasetuspto-grants-2014_02
ORD IDord-a2d22edcec944c5bbc04cf379c179a9e
Source noteuspto-grants-2014_02