tert-butyl N-[(2S)-1-[4-[4-[(5-chloro-4-pyrazolo[1,5-a]pyridin-3-ylpyrimidin-2-yl)amino]-5-methoxy-2-nitrophenyl]piperazin-1-yl]-1-oxopropan-2-yl]carbamate

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Chemical Name:tert-butyl N-[(2S)-1-[4-[4-[(5-chloro-4-pyrazolo[1,5-a]pyridin-3-ylpyrimidin-2-yl)amino]-5-methoxy-2-nitrophenyl]piperazin-1-yl]-1-oxopropan-2-yl]carbamate
CAS No.:1421372-26-0
Molecular Formula:C₃₀H₃₄ClN₉O₆
Molecular Weight:652.11
Hs Code.:

tert-butyl N-[(2S)-1-[4-[4-[(5-chloro-4-pyrazolo[1,5-a]pyridin-3-ylpyrimidin-2-yl)amino]-5-methoxy-2-nitrophenyl]piperazin-1-yl]-1-oxopropan-2-yl]carbamate

Synonyms:tert-butyl N-[(2S)-1-[4-[4-[(5-chloro-4-pyrazolo[1,5-a]pyridin-3-ylpyrimidin-2-yl)amino]-5-methoxy-2-nitrophenyl]piperazin-1-yl]-1-oxopropan-2-yl]carbamate

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Chemical Property of tert-butyl N-[(2S)-1-[4-[4-[(5-chloro-4-pyrazolo[1,5-a]pyridin-3-ylpyrimidin-2-yl)amino]-5-methoxy-2-nitrophenyl]piperazin-1-yl]-1-oxopropan-2-yl]carbamate

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Technology Process of tert-butyl N-[(2S)-1-[4-[4-[(5-chloro-4-pyrazolo[1,5-a]pyridin-3-ylpyrimidin-2-yl)amino]-5-methoxy-2-nitrophenyl]piperazin-1-yl]-1-oxopropan-2-yl]carbamate

There total 5 articles about tert-butyl N-[(2S)-1-[4-[4-[(5-chloro-4-pyrazolo[1,5-a]pyridin-3-ylpyrimidin-2-yl)amino]-5-methoxy-2-nitrophenyl]piperazin-1-yl]-1-oxopropan-2-yl]carbamate 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: 34.0%

: 1421372-08-8
5-chloro-N-(4-fluoro-2-methoxy-5-nitrophenyl)-4-(pyrazolo[1,5-a]pyridin-3-yl)pyrimidin-2-amine

: 205189-94-2
(S)-tert-butyl 1-oxo-1-(piperazin-1-yl)propan-2-ylcarbamate

: 1421372-26-0
tert-butyl N-[(2S)-1-[4-[4-[(5-chloro-4-pyrazolo[1,5-a]pyridin-3-ylpyrimidin-2-yl)amino]-5-methoxy-2-nitrophenyl]piperazin-1-yl]-1-oxopropan-2-yl]carbamate

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In 2,2,2-trifluoroethanol; at 140 ℃; for 1h; Microwave irradiation;

Reference yield:

: 1224709-13-0
3-(2,5-dichloropyrimidin-4-yl)pyrazolo[1,5-a]pyridine

: 1421372-26-0
tert-butyl N-[(2S)-1-[4-[4-[(5-chloro-4-pyrazolo[1,5-a]pyridin-3-ylpyrimidin-2-yl)amino]-5-methoxy-2-nitrophenyl]piperazin-1-yl]-1-oxopropan-2-yl]carbamate

Guidance literature:: Multi-step reaction with 2 steps

1: toluene-4-sulfonic acid / 18 h / 125 °C

2: N-ethyl-N,N-diisopropylamine / 2,2,2-trifluoroethanol / 1 h / 140 °C / Microwave irradiation

With toluene-4-sulfonic acid; N-ethyl-N,N-diisopropylamine; In 2,2,2-trifluoroethanol;

Reference yield:

: 1224708-12-6
4-[(E)-2-butoxyethenyl]-2,5-dichloropyrimidine

: 1421372-26-0
tert-butyl N-[(2S)-1-[4-[4-[(5-chloro-4-pyrazolo[1,5-a]pyridin-3-ylpyrimidin-2-yl)amino]-5-methoxy-2-nitrophenyl]piperazin-1-yl]-1-oxopropan-2-yl]carbamate

Guidance literature:: Multi-step reaction with 3 steps

1: potassium hydroxide; potassium carbonate / dimethyl sulfoxide / 5.5 h / 20 - 90 °C

2: toluene-4-sulfonic acid / 18 h / 125 °C

3: N-ethyl-N,N-diisopropylamine / 2,2,2-trifluoroethanol / 1 h / 140 °C / Microwave irradiation

With potassium carbonate; toluene-4-sulfonic acid; N-ethyl-N,N-diisopropylamine; potassium hydroxide; In 2,2,2-trifluoroethanol; dimethyl sulfoxide;