tert-butyl N-(2-{4-[1-(4-chlorophenyl)-1H-pyrrolo[2,3-c]pyridin-3-yl]piperidin-1-yl}-2-oxoethyl)carbamate

Base Information

Chemical Name:tert-butyl N-(2-{4-[1-(4-chlorophenyl)-1H-pyrrolo[2,3-c]pyridin-3-yl]piperidin-1-yl}-2-oxoethyl)carbamate
CAS No.:1334713-85-7
Molecular Formula:C₂₅H₂₉ClN₄O₃
Molecular Weight:468.983
Hs Code.:

Synonyms:tert-butyl N-(2-{4-[1-(4-chlorophenyl)-1H-pyrrolo[2,3-c]pyridin-3-yl]piperidin-1-yl}-2-oxoethyl)carbamate

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Chemical Property of tert-butyl N-(2-{4-[1-(4-chlorophenyl)-1H-pyrrolo[2,3-c]pyridin-3-yl]piperidin-1-yl}-2-oxoethyl)carbamate

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Technology Process of tert-butyl N-(2-{4-[1-(4-chlorophenyl)-1H-pyrrolo[2,3-c]pyridin-3-yl]piperidin-1-yl}-2-oxoethyl)carbamate

There total 6 articles about tert-butyl N-(2-{4-[1-(4-chlorophenyl)-1H-pyrrolo[2,3-c]pyridin-3-yl]piperidin-1-yl}-2-oxoethyl)carbamate 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: 41.0%

: 4530-20-5
BOC-glycine

: 1334711-87-3
1-(4-chlorophenyl)-3-piperidin-4-yl-1H-pyrrolo[2,3-c]pyridine trifluoroacetate

: 1334713-85-7
tert-butyl N-(2-{4-[1-(4-chlorophenyl)-1H-pyrrolo[2,3-c]pyridin-3-yl]piperidin-1-yl}-2-oxoethyl)carbamate

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In tetrahydrofuran; methanol;

Reference yield:

: 271-29-4
6-azaindole

: 1334713-85-7
tert-butyl N-(2-{4-[1-(4-chlorophenyl)-1H-pyrrolo[2,3-c]pyridin-3-yl]piperidin-1-yl}-2-oxoethyl)carbamate

Guidance literature:: Multi-step reaction with 5 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

4: dichloromethane / 2 h

5: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / tetrahydrofuran; methanol

With potassium phosphate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; potassium hydroxide; cyclohexene; copper(l) iodide; palladium 10% on activated carbon; N,N-dimethylethylenediamine; In tetrahydrofuran; methanol; ethanol; dichloromethane; toluene; 3: Buchwald-Hartwig Reaction;

Reference yield:

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

: 1334713-85-7
tert-butyl N-(2-{4-[1-(4-chlorophenyl)-1H-pyrrolo[2,3-c]pyridin-3-yl]piperidin-1-yl}-2-oxoethyl)carbamate

Guidance literature:: Multi-step reaction with 5 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

4: dichloromethane / 2 h

5: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / tetrahydrofuran; methanol

With potassium phosphate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; potassium hydroxide; cyclohexene; copper(l) iodide; palladium 10% on activated carbon; N,N-dimethylethylenediamine; In tetrahydrofuran; methanol; ethanol; dichloromethane; toluene; 3: Buchwald-Hartwig Reaction;