4-[4-(3-Benzyl-3H-imidazo[4,5-b]pyridin-2-ylamino)-piperidin-1-yl]-N,N-dimethyl-2,2-diphenyl-butyramide

Base Information

Chemical Name:4-[4-(3-Benzyl-3H-imidazo[4,5-b]pyridin-2-ylamino)-piperidin-1-yl]-N,N-dimethyl-2,2-diphenyl-butyramide
CAS No.:98331-30-7
Molecular Formula:C₃₆H₄₀N₆O
Molecular Weight:572.753
Hs Code.:

Synonyms:4-[4-(3-Benzyl-3H-imidazo[4,5-b]pyridin-2-ylamino)-piperidin-1-yl]-N,N-dimethyl-2,2-diphenyl-butyramide

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Chemical Property of 4-[4-(3-Benzyl-3H-imidazo[4,5-b]pyridin-2-ylamino)-piperidin-1-yl]-N,N-dimethyl-2,2-diphenyl-butyramide

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Technology Process of 4-[4-(3-Benzyl-3H-imidazo[4,5-b]pyridin-2-ylamino)-piperidin-1-yl]-N,N-dimethyl-2,2-diphenyl-butyramide

There total 7 articles about 4-[4-(3-Benzyl-3H-imidazo[4,5-b]pyridin-2-ylamino)-piperidin-1-yl]-N,N-dimethyl-2,2-diphenyl-butyramide 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: 61.0%

: Methanesulfonic acid 3-dimethylcarbamoyl-3,3-diphenyl-propyl ester

: 76031-50-0
3-(phenylmethyl)-N-(4-piperidinyl)-3H-imidazo[4,5-b]pyridin-2-amine

: 98331-30-7
4-[4-(3-Benzyl-3H-imidazo[4,5-b]pyridin-2-ylamino)-piperidin-1-yl]-N,N-dimethyl-2,2-diphenyl-butyramide

Guidance literature:: With sodium carbonate; In N,N-dimethyl-formamide; at 70 ℃; for 20h;
DOI:10.1021/jm00150a030

Reference yield:

: 3723-70-4
benzyl-(3-nitro-pyridin-2-yl)-amine

: 98331-30-7
4-[4-(3-Benzyl-3H-imidazo[4,5-b]pyridin-2-ylamino)-piperidin-1-yl]-N,N-dimethyl-2,2-diphenyl-butyramide

Guidance literature:: Multi-step reaction with 5 steps

1: H₂ / RaNi / methanol / 760 Torr / Ambient temperature

2: 70 percent / methanol

3: 50 percent / HgO/S / tetrahydrofuran / Heating

4: 48 percent aq. HBr / 70 °C

5: 61 percent / sodium carbonate / dimethylformamide / 20 h / 70 °C

With hydrogen bromide; hydrogen; sodium carbonate; sulfur; mercury(II) oxide; RaNi; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;
DOI:10.1021/jm00150a030

Reference yield:

: 5470-18-8,34515-82-7
2-Chloro-3-nitropyridine

: 98331-30-7
4-[4-(3-Benzyl-3H-imidazo[4,5-b]pyridin-2-ylamino)-piperidin-1-yl]-N,N-dimethyl-2,2-diphenyl-butyramide

Guidance literature:: Multi-step reaction with 6 steps

1: 80 percent / sodium carbonate / dimethylformamide / 1 h / Heating

2: H₂ / RaNi / methanol / 760 Torr / Ambient temperature

3: 70 percent / methanol

4: 50 percent / HgO/S / tetrahydrofuran / Heating

5: 48 percent aq. HBr / 70 °C

6: 61 percent / sodium carbonate / dimethylformamide / 20 h / 70 °C

With hydrogen bromide; hydrogen; sodium carbonate; sulfur; mercury(II) oxide; RaNi; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;
DOI:10.1021/jm00150a030