tert-butyl 4-[1-(4-chlorophenyl)-1H-pyrrolo[2,3-c]pyridin-3-yl]piperidine-1-carboxylate

Base Information

Chemical Name:tert-butyl 4-[1-(4-chlorophenyl)-1H-pyrrolo[2,3-c]pyridin-3-yl]piperidine-1-carboxylate
CAS No.:1334711-85-1
Molecular Formula:C₂₃H₂₆ClN₃O₂
Molecular Weight:411.931
Hs Code.:

Synonyms:tert-butyl 4-[1-(4-chlorophenyl)-1H-pyrrolo[2,3-c]pyridin-3-yl]piperidine-1-carboxylate

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Chemical Property of tert-butyl 4-[1-(4-chlorophenyl)-1H-pyrrolo[2,3-c]pyridin-3-yl]piperidine-1-carboxylate

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Technology Process of tert-butyl 4-[1-(4-chlorophenyl)-1H-pyrrolo[2,3-c]pyridin-3-yl]piperidine-1-carboxylate

There total 4 articles about tert-butyl 4-[1-(4-chlorophenyl)-1H-pyrrolo[2,3-c]pyridin-3-yl]piperidine-1-carboxylate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 89.0%

: tert-butyl 4-{1H-pyrrolo[2,3-c]pyridin-3-yl}piperidine-1-carboxylate

: 637-87-6
1-Chloro-4-iodobenzene

: 1334711-85-1
tert-butyl 4-[1-(4-chlorophenyl)-1H-pyrrolo[2,3-c]pyridin-3-yl]piperidine-1-carboxylate

Guidance literature:: With potassium phosphate; copper(l) iodide; N,N-dimethylethylenediamine; In toluene; at 110 ℃; for 72h;

Reference yield:

: 271-29-4
6-azaindole

: 1334711-85-1
tert-butyl 4-[1-(4-chlorophenyl)-1H-pyrrolo[2,3-c]pyridin-3-yl]piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: potassium hydroxide / methanol / Reflux

2: cyclohexene / palladium 10% on activated carbon / ethanol / 0.42 h / 150 °C / Microwave irradiation

3: potassium phosphate / copper(l) iodide; N,N-dimethylethylenediamine / toluene / 72 h / 110 °C

With potassium phosphate; potassium hydroxide; cyclohexene; copper(l) iodide; palladium 10% on activated carbon; N,N-dimethylethylenediamine; In methanol; ethanol; toluene; 3: Buchwald-Hartwig Reaction;

Reference yield:

: 79099-07-3
N-tert-butyloxycarbonylpiperidin-4-one

: 1334711-85-1
tert-butyl 4-[1-(4-chlorophenyl)-1H-pyrrolo[2,3-c]pyridin-3-yl]piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: potassium hydroxide / methanol / Reflux

2: cyclohexene / palladium 10% on activated carbon / ethanol / 0.42 h / 150 °C / Microwave irradiation

3: potassium phosphate / copper(l) iodide; N,N-dimethylethylenediamine / toluene / 72 h / 110 °C

With potassium phosphate; potassium hydroxide; cyclohexene; copper(l) iodide; palladium 10% on activated carbon; N,N-dimethylethylenediamine; In methanol; ethanol; toluene; 3: Buchwald-Hartwig Reaction;