Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1406417Generated: October 26, 2026

tert-Butyl 5-(4-methylpiperazin-1-yl)-1H-indole-1-carboxylate → 5-(4-Methyl-piperazin-1-yl)-2-[5-nitro-2-oxo-1-(2-trimethylsilanyl-ethoxymethyl)-1,2-dihydro-pyridin-3-yl]-indole-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1406417

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 5-(4-methylpiperazin-1-yl)-1H-indole-1-carboxylateHCID 58117405—
Reactant3-iodo-5-nitro-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyridin-2-oneHCID 58117411—
Product5-(4-Methyl-piperazin-1-yl)-2-[5-nitro-2-oxo-1-(2-trimethylsilanyl-ethoxymethyl)-1,2-dihydro-pyridin-3-yl]-indole-1-carboxylic acid tert-butyl esterHCID 58117412—

Reaction Steps

The title compound was prepared by the route outlined in Scheme 10 and using the experimental from Example 37, Step 3, with intermediate (10c), 5-(4-methyl-piperazin-1-yl)-indole-1-carboxylic acid tert-butyl ester (2.33 g, 7.4 mmol) and 3-iodo-5-nitro-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyridin-2-one (2.66 g, 6.7 mmol) which had been synthesised according to the protocol described for intermediate (6a) in example 20. The resultant solid was purified via trituration using diethyl ether, to afford the title compound as a pale brown solid, 1.73 g, 40%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916591B2
Source datasetuspto-grants-2014_12
ORD IDord-3f53cc8045844701b473bf3608aa12f9
Source noteuspto-grants-2014_12