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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32408Generated: October 29, 2026

3-Chloro-1H-indole-6-carboxylic acid → 4-(2-[(3-chloro-1H-indole-6-carbonyl)amino]-2-(4-pyridinyl)ethoxymethyl}piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/32408

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-1H-indole-6-carboxylic acidHCID 15543042—
Reactant4-[2-Amino-2-(4-pyridinyl)-ethoxymethyl]piperidine-1-carboxylic acid tert-butyl esterHCID 69309620—
Product4-(2-[(3-chloro-1H-indole-6-carbonyl)amino]-2-(4-pyridinyl)ethoxymethyl}piperidine-1-carboxylic acid tert-butyl esterHCID 69310608—

Reaction Steps

Using coupling method A, 4-[2-amino-2-(4-pyridinyl)-ethoxymethyl]piperidine-1-carboxylic acid tert-butyl ester (233 mg, 0.69 mmol) and 3-chloroindole-6-carboxylic acid (149 mg, 0.76 mmol) afforded, after purification (SiO2: 10 DCM:2 EtOAc:2 Hexane:3 isopropyl amine), 118 mg (33%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07427632B2
Source datasetuspto-grants-2008_09
ORD IDord-71effe43a5fa4eafac56168097754c2d
Source noteuspto-grants-2008_09