[(R)-1-(3-{[1-(4-fluorobenzyl)-1H-pyrazole-4-carbonyl]amino}-5-methoxy-1H-pyrrolo[2,3-b]pyridin-4-yl)piperidin-3-yl]carbamic acid tert-butyl ester

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Chemical Name:[(R)-1-(3-{[1-(4-fluorobenzyl)-1H-pyrazole-4-carbonyl]amino}-5-methoxy-1H-pyrrolo[2,3-b]pyridin-4-yl)piperidin-3-yl]carbamic acid tert-butyl ester
CAS No.:1449321-50-9
Molecular Formula:C₂₉H₃₄FN₇O₄
Molecular Weight:563.632
Hs Code.:

Synonyms:[(R)-1-(3-{[1-(4-fluorobenzyl)-1H-pyrazole-4-carbonyl]amino}-5-methoxy-1H-pyrrolo[2,3-b]pyridin-4-yl)piperidin-3-yl]carbamic acid tert-butyl ester

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Chemical Property of [(R)-1-(3-{[1-(4-fluorobenzyl)-1H-pyrazole-4-carbonyl]amino}-5-methoxy-1H-pyrrolo[2,3-b]pyridin-4-yl)piperidin-3-yl]carbamic acid tert-butyl ester

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Technology Process of [(R)-1-(3-{[1-(4-fluorobenzyl)-1H-pyrazole-4-carbonyl]amino}-5-methoxy-1H-pyrrolo[2,3-b]pyridin-4-yl)piperidin-3-yl]carbamic acid tert-butyl ester

There total 3 articles about [(R)-1-(3-{[1-(4-fluorobenzyl)-1H-pyrazole-4-carbonyl]amino}-5-methoxy-1H-pyrrolo[2,3-b]pyridin-4-yl)piperidin-3-yl]carbamic 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: 57.2%

: 1154881-57-8
1-(4-fluorobenzyl)-1H-pyrazole-4-carboxylic acid

: 1449319-50-9
[(R)-1-(3-amino-5-methoxy-1H-pyrrolo[2,3-b]pyridin-4-yl)piperidin-3-yl]carbamic acid tert-butyl ester

: 1449321-50-9
[(R)-1-(3-{[1-(4-fluorobenzyl)-1H-pyrazole-4-carbonyl]amino}-5-methoxy-1H-pyrrolo[2,3-b]pyridin-4-yl)piperidin-3-yl]carbamic acid tert-butyl ester

Guidance literature:: With triethylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In N,N-dimethyl-formamide; at 20 ℃; for 18h;

Reference yield:

: 459-46-1
4-Fluorobenzyl bromide

: 1449321-50-9
[(R)-1-(3-{[1-(4-fluorobenzyl)-1H-pyrazole-4-carbonyl]amino}-5-methoxy-1H-pyrrolo[2,3-b]pyridin-4-yl)piperidin-3-yl]carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate / acetone / 18 h / 50 °C

2: potassium hydroxide; water / methanol / 2 h / Reflux

3: triethylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / N,N-dimethyl-formamide / 18 h / 20 °C

With water; potassium carbonate; triethylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; potassium hydroxide; In methanol; N,N-dimethyl-formamide; acetone;

Reference yield:

: 1094202-69-3
ethyl 1-(4-fluorobenzyl)-1H-pyrazole-4-carboxylate

: 1449321-50-9
[(R)-1-(3-{[1-(4-fluorobenzyl)-1H-pyrazole-4-carbonyl]amino}-5-methoxy-1H-pyrrolo[2,3-b]pyridin-4-yl)piperidin-3-yl]carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: potassium hydroxide; water / methanol / 2 h / Reflux

2: triethylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / N,N-dimethyl-formamide / 18 h / 20 °C

With water; triethylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; potassium hydroxide; In methanol; N,N-dimethyl-formamide;