Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173244Generated: October 30, 2026

tert-Butyl piperazine-1-carboxylate → 1-(piperazin-1-ylmethyl)-2,3-dihydro-1H-indene-4-carbonitrile

https://huagongshe.com/reaction/2173244

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant1-formyl-2,3-dihydro-1H-indene-4-carbonitrileHCID 59568698—
SolventBenzonitrileHCID 7505—
Product1-(piperazin-1-ylmethyl)-2,3-dihydro-1H-indene-4-carbonitrileHCID 67517019—

Reaction Steps

1-(Piperazin-1-ylmethyl)-2,3-dihydro-1H-indene-4-carbonitrile was prepared starting from 1-formyl-2,3-dihydro-1H-indene-4-carbonitrile and tert-butyl piperazine-1-carboxylate in two steps in an analogous fashion to that described for the synthesis of 2-methoxy-4-[2-piperazin-1-yl)ethyl]benzonitrile above. 1H-NMR (400 MHz, MeOD) δ ppm 7.68 (d, J=7.8 Hz, 1H), 7.58 (d, J=7.8 Hz, 1H), 7.40 (t, J=7.4 Hz, 1H), 3.64˜3.88 (m, 10H), 3.40˜3.46 (m, 1H), 3.20˜3.30 (m, 1H), 3.07˜3.16 (m, 1H), 2.55˜2.70 (m, 1H), 2.10˜2.25 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056859B2
Source datasetuspto-grants-2015_06
ORD IDord-297aa3548f69496084e6a60abe7f087b
Source noteuspto-grants-2015_06