2-[(4-{2-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]butyl}piperazin-1-yl)carbonyl]phenol

Base Information

Chemical Name:2-[(4-{2-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]butyl}piperazin-1-yl)carbonyl]phenol
CAS No.:1270979-88-8
Molecular Formula:C₂₄H₂₇N₇O₂
Molecular Weight:445.524
Hs Code.:

Synonyms:2-[(4-{2-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]butyl}piperazin-1-yl)carbonyl]phenol

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Chemical Property of 2-[(4-{2-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]butyl}piperazin-1-yl)carbonyl]phenol

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Technology Process of 2-[(4-{2-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]butyl}piperazin-1-yl)carbonyl]phenol

There total 5 articles about 2-[(4-{2-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]butyl}piperazin-1-yl)carbonyl]phenol 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:

: 1270981-86-6
4-{1-[1-(piperazin-1-ylmethyl)propyl]-1H-pyrazol-4-yl}-7-{[2-(trimethylsilyl)ethoxy]methyl}-7H-pyrrolo[2,3-d]pyrimidine

: 69-72-7,25496-36-0,8052-31-1
salicylic acid

: 1270979-88-8
2-[(4-{2-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]butyl}piperazin-1-yl)carbonyl]phenol

Guidance literature:: salicylic acid; With N-ethyl-N,N-diisopropylamine; HATU; In tetrahydrofuran; for 1h;

4-{1-[1-(piperazin-1-ylmethyl)propyl]-1H-pyrazol-4-yl}-7-{[2-(trimethylsilyl)ethoxy]methyl}-7H-pyrrolo[2,3-d]pyrimidine; In tetrahydrofuran; for 0.5h;

With trifluoroacetic acid; In tetrahydrofuran; for 0.5h;

Reference yield:

: 941685-27-4
4-(1H-pyrazol-4-yl)-7-((2-trimethylsilanylethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidine

: 1270979-88-8
2-[(4-{2-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]butyl}piperazin-1-yl)carbonyl]phenol

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydride / N,N-dimethyl-formamide / 0.25 h / 0 °C

1.2: 4.5 h

2.1: diisobutylaluminium hydride / toluene / -78 - -55 °C

3.1: dichloromethane / 1.6 h

3.2: 1 h

4.1: hydrogenchloride / 1,4-dioxane / 1 h

5.1: N-ethyl-N,N-diisopropylamine; HATU / tetrahydrofuran / 1 h

5.2: 0.5 h

5.3: 0.5 h

With hydrogenchloride; sodium hydride; diisobutylaluminium hydride; N-ethyl-N,N-diisopropylamine; HATU; In tetrahydrofuran; 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide; toluene;

Reference yield:

: 1270981-82-2
ethyl 2-(4-(7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl)butanoate

: 1270979-88-8
2-[(4-{2-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]butyl}piperazin-1-yl)carbonyl]phenol

Guidance literature:: Multi-step reaction with 4 steps

1.1: diisobutylaluminium hydride / toluene / -78 - -55 °C

2.1: dichloromethane / 1.6 h

2.2: 1 h

3.1: hydrogenchloride / 1,4-dioxane / 1 h

4.1: N-ethyl-N,N-diisopropylamine; HATU / tetrahydrofuran / 1 h

4.2: 0.5 h

4.3: 0.5 h

With hydrogenchloride; diisobutylaluminium hydride; N-ethyl-N,N-diisopropylamine; HATU; In tetrahydrofuran; 1,4-dioxane; dichloromethane; toluene;