1,1-dimethylethyl 4-(4-amino-5-(1-[(2,5-difluorophenyl)acetyl]-2,3-dihydro-1H-indol-5-yl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-1-piperidinecarboxylate

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Chemical Name:1,1-dimethylethyl 4-(4-amino-5-(1-[(2,5-difluorophenyl)acetyl]-2,3-dihydro-1H-indol-5-yl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-1-piperidinecarboxylate
CAS No.:1337533-02-4
Molecular Formula:C₃₂H₃₄F₂N₆O₃
Molecular Weight:588.657
Hs Code.:

Synonyms:1,1-dimethylethyl 4-(4-amino-5-(1-[(2,5-difluorophenyl)acetyl]-2,3-dihydro-1H-indol-5-yl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-1-piperidinecarboxylate

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Chemical Property of 1,1-dimethylethyl 4-(4-amino-5-(1-[(2,5-difluorophenyl)acetyl]-2,3-dihydro-1H-indol-5-yl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-1-piperidinecarboxylate

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Technology Process of 1,1-dimethylethyl 4-(4-amino-5-(1-[(2,5-difluorophenyl)acetyl]-2,3-dihydro-1H-indol-5-yl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-1-piperidinecarboxylate

There total 5 articles about 1,1-dimethylethyl 4-(4-amino-5-(1-[(2,5-difluorophenyl)acetyl]-2,3-dihydro-1H-indol-5-yl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-1-piperidinecarboxylate 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:

: 1337532-99-6
1,1-dimethylethyl 4-(4-amino-5-bromo-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-1-piperidinecarboxylate

: 1337533-26-2
1-[(2,5-difluorophenyl)acetyl]-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-dihydro-1H-indole

: 1337533-02-4
1,1-dimethylethyl 4-(4-amino-5-(1-[(2,5-difluorophenyl)acetyl]-2,3-dihydro-1H-indol-5-yl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-1-piperidinecarboxylate

Guidance literature:: With sodium hydrogencarbonate; triphenylphosphine; In 1,4-dioxane; water; at 120 ℃; for 4h; Inert atmosphere;

Reference yield:

: 22276-95-5
5-bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidine

: 1337533-02-4
1,1-dimethylethyl 4-(4-amino-5-(1-[(2,5-difluorophenyl)acetyl]-2,3-dihydro-1H-indol-5-yl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-1-piperidinecarboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 2 h / 20 °C

2: ammonium hydroxide / 1,4-dioxane / 0.75 h / 100 °C / Microwave irradiation

3: sodium hydrogencarbonate / triphenylphosphine / 1,4-dioxane; water / 4 h / 120 °C / Inert atmosphere

With ammonium hydroxide; sodium hydrogencarbonate; triphenylphosphine; diethylazodicarboxylate; triphenylphosphine; In tetrahydrofuran; 1,4-dioxane; water;

Reference yield:

: 3680-69-1
4-chloro-1H-pyrrolo[2,3-d]pyrimidine

: 1337533-02-4
1,1-dimethylethyl 4-(4-amino-5-(1-[(2,5-difluorophenyl)acetyl]-2,3-dihydro-1H-indol-5-yl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-1-piperidinecarboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: N-Bromosuccinimide / chloroform / 3 h / 20 - 70 °C

2: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 2 h / 20 °C

3: ammonium hydroxide / 1,4-dioxane / 0.75 h / 100 °C / Microwave irradiation

4: sodium hydrogencarbonate / triphenylphosphine / 1,4-dioxane; water / 4 h / 120 °C / Inert atmosphere

With ammonium hydroxide; N-Bromosuccinimide; sodium hydrogencarbonate; triphenylphosphine; diethylazodicarboxylate; triphenylphosphine; In tetrahydrofuran; 1,4-dioxane; chloroform; water;