1-benzyl-N-{5-bromo-4-[(R)-3-(cyclopentylmethylamino)piperidin-1-yl]-1H-pyrrolo[2,3-b]pyridin-3-yl}-1H-pyrazole-4-carboxylic acid amide

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Chemical Name:1-benzyl-N-{5-bromo-4-[(R)-3-(cyclopentylmethylamino)piperidin-1-yl]-1H-pyrrolo[2,3-b]pyridin-3-yl}-1H-pyrazole-4-carboxylic acid amide
CAS No.:1449318-70-0
Molecular Formula:C₂₉H₃₄BrN₇O
Molecular Weight:576.539
Hs Code.:

Synonyms:1-benzyl-N-{5-bromo-4-[(R)-3-(cyclopentylmethylamino)piperidin-1-yl]-1H-pyrrolo[2,3-b]pyridin-3-yl}-1H-pyrazole-4-carboxylic acid amide

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Chemical Property of 1-benzyl-N-{5-bromo-4-[(R)-3-(cyclopentylmethylamino)piperidin-1-yl]-1H-pyrrolo[2,3-b]pyridin-3-yl}-1H-pyrazole-4-carboxylic acid amide

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Technology Process of 1-benzyl-N-{5-bromo-4-[(R)-3-(cyclopentylmethylamino)piperidin-1-yl]-1H-pyrrolo[2,3-b]pyridin-3-yl}-1H-pyrazole-4-carboxylic acid amide

There total 4 articles about 1-benzyl-N-{5-bromo-4-[(R)-3-(cyclopentylmethylamino)piperidin-1-yl]-1H-pyrrolo[2,3-b]pyridin-3-yl}-1H-pyrazole-4-carboxylic acid amide 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: 12.1%

: 872-53-7
cyclopentanealdehyde

: 1449318-47-1
1-benzyl-1H-pyrazol-4-carboxylic acid [4-((R)-3-aminopiperidin-1-yl)-5-bromo-1H-pyrrolo[2,3-b]pyridin-3-yl]amide

: 1449318-70-0
1-benzyl-N-{5-bromo-4-[(R)-3-(cyclopentylmethylamino)piperidin-1-yl]-1H-pyrrolo[2,3-b]pyridin-3-yl}-1H-pyrazole-4-carboxylic acid amide

Guidance literature:: cyclopentanealdehyde; 1-benzyl-1H-pyrazol-4-carboxylic acid [4-((R)-3-aminopiperidin-1-yl)-5-bromo-1H-pyrrolo[2,3-b]pyridin-3-yl]amide; With acetic acid; In methanol; at 20 ℃; for 0.166667h;

With sodium tris(acetoxy)borohydride; In methanol; at 20 ℃; for 18h;

Reference yield:

: 1449318-54-0
1-benzyl-1H-pyrazol-4-carboxylic acid (5-bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridin-3-yl)amide

: 1449318-70-0
1-benzyl-N-{5-bromo-4-[(R)-3-(cyclopentylmethylamino)piperidin-1-yl]-1H-pyrrolo[2,3-b]pyridin-3-yl}-1H-pyrazole-4-carboxylic acid amide

Guidance literature:: Multi-step reaction with 3 steps

1.1: butan-1-ol / 8 h / 160 °C / Microwave irradiation

2.1: trifluoroacetic acid / dichloromethane / 3 h / 20 °C

3.1: acetic acid / methanol / 0.17 h / 20 °C

3.2: 18 h / 20 °C

With acetic acid; trifluoroacetic acid; In methanol; dichloromethane; butan-1-ol;

Reference yield:

: 309956-78-3,172603-05-3
(R)-piperidin-3-ylcarbamic acid tert-butyl ester

: 1449318-70-0
1-benzyl-N-{5-bromo-4-[(R)-3-(cyclopentylmethylamino)piperidin-1-yl]-1H-pyrrolo[2,3-b]pyridin-3-yl}-1H-pyrazole-4-carboxylic acid amide

Guidance literature:: Multi-step reaction with 3 steps

1.1: butan-1-ol / 8 h / 160 °C / Microwave irradiation

2.1: trifluoroacetic acid / dichloromethane / 3 h / 20 °C

3.1: acetic acid / methanol / 0.17 h / 20 °C

3.2: 18 h / 20 °C

With acetic acid; trifluoroacetic acid; In methanol; dichloromethane; butan-1-ol;