tert-butyl 4-(7-(methyl(4-(methylsulfonyl)phenyl)amino)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-3-yl)piperidine-1-carboxylate

Base Information

Chemical Name:tert-butyl 4-(7-(methyl(4-(methylsulfonyl)phenyl)amino)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-3-yl)piperidine-1-carboxylate
CAS No.:1313029-40-1
Molecular Formula:C₂₂H₂₉N₇O₄S
Molecular Weight:487.583
Hs Code.:

Synonyms:tert-butyl 4-(7-(methyl(4-(methylsulfonyl)phenyl)amino)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-3-yl)piperidine-1-carboxylate

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Chemical Property of tert-butyl 4-(7-(methyl(4-(methylsulfonyl)phenyl)amino)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-3-yl)piperidine-1-carboxylate

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Technology Process of tert-butyl 4-(7-(methyl(4-(methylsulfonyl)phenyl)amino)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-3-yl)piperidine-1-carboxylate

There total 4 articles about tert-butyl 4-(7-(methyl(4-(methylsulfonyl)phenyl)amino)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-3-yl)piperidine-1-carboxylate 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:

: 1313029-73-0
C₂₂H₃₂N₆O₄S

: 1313029-40-1
tert-butyl 4-(7-(methyl(4-(methylsulfonyl)phenyl)amino)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-3-yl)piperidine-1-carboxylate

Guidance literature:: With acetic acid; sodium nitrite; at 20 ℃; for 2h;

Reference yield:

: 119871-25-9
N-methyl-4-(methylsulfonyl)benzenamine

: 1313029-40-1
tert-butyl 4-(7-(methyl(4-(methylsulfonyl)phenyl)amino)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-3-yl)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 5 h / 0 - 20 °C

2: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 5 h / 0 - 20 °C

3: hydrogen / palladium 10% on activated carbon / methanol / 2 h / 20 °C

4: sodium nitrite; acetic acid / 2 h / 20 °C

With hydrogen; acetic acid; N-ethyl-N,N-diisopropylamine; sodium nitrite; palladium 10% on activated carbon; In tetrahydrofuran; methanol;

Reference yield:

: 1313029-41-2
6-chloro-N-methyl-N-(4-(methylsulfonyl)phenyl)-5-nitropyrimidin-4-amine

: 1313029-40-1
tert-butyl 4-(7-(methyl(4-(methylsulfonyl)phenyl)amino)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-3-yl)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 5 h / 0 - 20 °C

2: hydrogen / palladium 10% on activated carbon / methanol / 2 h / 20 °C

3: sodium nitrite; acetic acid / 2 h / 20 °C

With hydrogen; acetic acid; N-ethyl-N,N-diisopropylamine; sodium nitrite; palladium 10% on activated carbon; In tetrahydrofuran; methanol;