4-(1H-Pyrrolo[2,3-b]pyridin-3-yl)-piperidine-1-carboxylic acid tert-butyl ester

Base Information

Chemical Name:4-(1H-Pyrrolo[2,3-b]pyridin-3-yl)-piperidine-1-carboxylic acid tert-butyl ester
CAS No.:1001414-23-8
Molecular Formula:C₁₈H₂₅N₃O₂
Molecular Weight:315.415
Hs Code.:
Mol file:1001414-23-8.mol

Synonyms:4-(1H-Pyrrolo[2,3-b]pyridin-3-yl)-piperidine-1-carboxylic acid tert-butyl ester

Suppliers and Price of 4-(1H-Pyrrolo[2,3-b]pyridin-3-yl)-piperidine-1-carboxylic acid tert-butyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Total 1 raw suppliers

Chemical Property of 4-(1H-Pyrrolo[2,3-b]pyridin-3-yl)-piperidine-1-carboxylic acid tert-butyl ester

Chemical Property:

Purity/Quality:: 99% ，98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 4-(1H-Pyrrolo[2,3-b]pyridin-3-yl)-piperidine-1-carboxylic acid tert-butyl ester

There total 3 articles about 4-(1H-Pyrrolo[2,3-b]pyridin-3-yl)-piperidine-1-carboxylic acid tert-butyl ester 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: 78.0%

: 1001414-20-5
tert-butyl N-[4-(1H-pyrrolo[2,3-b]pyridin-3-yl)cyclohex-3-en-1-yl]carbamate

: 1001414-23-8
[4-(1H-pyrrolo[2,3-b]pyridin-3-yl)-cyclohexyl]-carbamic acid tert-butyl ester

Guidance literature:: With hydrogen; palladium dihydroxide; In tetrahydrofuran; methanol; under 760.051 Torr;

Reference yield:

: 271-63-6
7-Azaindole

: 1001414-23-8
[4-(1H-pyrrolo[2,3-b]pyridin-3-yl)-cyclohexyl]-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: sodium ethanolate / ethanol / Heating / reflux

2: hydrogen / palladium dihydroxide / tetrahydrofuran; methanol / 760.05 Torr

With hydrogen; sodium ethanolate; palladium dihydroxide; In tetrahydrofuran; methanol; ethanol;

Reference yield:

: 179321-49-4
N-(tert-butoxycarbonyl)-4-aminocyclohexanone

: 1001414-23-8
[4-(1H-pyrrolo[2,3-b]pyridin-3-yl)-cyclohexyl]-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: sodium ethanolate / ethanol / Heating / reflux

2: hydrogen / palladium dihydroxide / tetrahydrofuran; methanol / 760.05 Torr

With hydrogen; sodium ethanolate; palladium dihydroxide; In tetrahydrofuran; methanol; ethanol;