4-(5-amino-1-benzenesulphonyl-1H-pyrrolo[2,3-b]pyridine-4ylamino)piperidine-1-carboxylic acid tert-butyl ester

Base Information

Chemical Name:4-(5-amino-1-benzenesulphonyl-1H-pyrrolo[2,3-b]pyridine-4ylamino)piperidine-1-carboxylic acid tert-butyl ester
CAS No.:1315495-07-8
Molecular Formula:C₂₃H₂₉N₅O₄S
Molecular Weight:471.58
Hs Code.:

Synonyms:4-(5-amino-1-benzenesulphonyl-1H-pyrrolo[2,3-b]pyridine-4ylamino)piperidine-1-carboxylic acid tert-butyl ester

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Chemical Property of 4-(5-amino-1-benzenesulphonyl-1H-pyrrolo[2,3-b]pyridine-4ylamino)piperidine-1-carboxylic acid tert-butyl ester

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

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Technology Process of 4-(5-amino-1-benzenesulphonyl-1H-pyrrolo[2,3-b]pyridine-4ylamino)piperidine-1-carboxylic acid tert-butyl ester

There total 6 articles about 4-(5-amino-1-benzenesulphonyl-1H-pyrrolo[2,3-b]pyridine-4ylamino)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: 82.0%

: 1315495-05-6
4-(1-benzenesulphonyl-5-nitro-1H-pyrrolo[2,3-b]pyridine-4ylamino)piperidine-1-carboxylic acid tert-butyl ester

: 1315495-07-8
4-(5-amino-1-benzenesulphonyl-1H-pyrrolo[2,3-b]pyridine-4ylamino)piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: With hydrogen; 20% palladium hydroxide-activated charcoal; In acetic acid; at 50 ℃; for 24h; Inert atmosphere;

Reference yield:

: 55052-28-3
4-chloro-7-azaindole

: 1315495-07-8
4-(5-amino-1-benzenesulphonyl-1H-pyrrolo[2,3-b]pyridine-4ylamino)piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine / dmap / dichloromethane / 18 - 25 °C

2: tetrabutylammonium nitrate; trifluoroacetic anhydride / dichloromethane / 23.5 h / -5 - 25 °C

3: N-ethyl-N,N-diisopropylamine / isopropyl alcohol / 2 h / Reflux

4: hydrogen / 20% palladium hydroxide-activated charcoal / acetic acid / 24 h / 50 °C / Inert atmosphere

With hydrogen; tetrabutylammonium nitrate; triethylamine; N-ethyl-N,N-diisopropylamine; trifluoroacetic anhydride; dmap; 20% palladium hydroxide-activated charcoal; In dichloromethane; acetic acid; isopropyl alcohol;

Reference yield:

: 1245649-52-8
1-(benzenesulfonyl)-4-chloro-5-nitro-1H-pyrrolo[2,3-b]pyridine

: 1315495-07-8
4-(5-amino-1-benzenesulphonyl-1H-pyrrolo[2,3-b]pyridine-4ylamino)piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: N-ethyl-N,N-diisopropylamine / isopropyl alcohol / 2 h / Reflux

2: hydrogen / 20% palladium hydroxide-activated charcoal / acetic acid / 24 h / 50 °C / Inert atmosphere

With hydrogen; N-ethyl-N,N-diisopropylamine; 20% palladium hydroxide-activated charcoal; In acetic acid; isopropyl alcohol;