2-((2-((R)-3-aminopiperidin-1-yl)-6-methyl-4-oxo-4,7-dihydro-3H-pyrrolo[2,3-d]pyrimidin-3-yl)methyl)benzonitrile

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Chemical Name:2-((2-((R)-3-aminopiperidin-1-yl)-6-methyl-4-oxo-4,7-dihydro-3H-pyrrolo[2,3-d]pyrimidin-3-yl)methyl)benzonitrile
CAS No.:1355173-69-1
Molecular Formula:C₂₀H₂₂N₆O
Molecular Weight:362.434
Hs Code.:

Synonyms:2-((2-((R)-3-aminopiperidin-1-yl)-6-methyl-4-oxo-4,7-dihydro-3H-pyrrolo[2,3-d]pyrimidin-3-yl)methyl)benzonitrile

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Chemical Property of 2-((2-((R)-3-aminopiperidin-1-yl)-6-methyl-4-oxo-4,7-dihydro-3H-pyrrolo[2,3-d]pyrimidin-3-yl)methyl)benzonitrile

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Technology Process of 2-((2-((R)-3-aminopiperidin-1-yl)-6-methyl-4-oxo-4,7-dihydro-3H-pyrrolo[2,3-d]pyrimidin-3-yl)methyl)benzonitrile

There total 3 articles about 2-((2-((R)-3-aminopiperidin-1-yl)-6-methyl-4-oxo-4,7-dihydro-3H-pyrrolo[2,3-d]pyrimidin-3-yl)methyl)benzonitrile 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: 72.0%

: 334618-23-4
3-(R)-aminopiperidine dihydrochloride

: 1355174-84-3
2-((2-chloro-6-methyl-4-oxo-4,7-dihydro-3H-pyrrolo[2,3-d]pyrimidin-3-yl)methyl)benzonitrile

: 1355173-69-1
2-((2-((R)-3-aminopiperidin-1-yl)-6-methyl-4-oxo-4,7-dihydro-3H-pyrrolo[2,3-d]pyrimidin-3-yl)methyl)benzonitrile

Guidance literature:: With sodium hydrogencarbonate; In ethanol; at 150 ℃; for 6h;
DOI:10.1016/j.ejmech.2012.03.015

Reference yield:

: 1192711-71-9
2,4-dichloro-6-methyl-7H-pyrrolo[2,3-d]pyrimidine

: 1355173-69-1
2-((2-((R)-3-aminopiperidin-1-yl)-6-methyl-4-oxo-4,7-dihydro-3H-pyrrolo[2,3-d]pyrimidin-3-yl)methyl)benzonitrile

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydroxide / water / 80 °C

1.2: pH 6

2.1: dmap; triethylamine / tetrahydrofuran / 0.5 h / 0 °C

2.2: 20 °C

3.1: sodium hydride / 1,2-dimethoxyethane; N,N-dimethyl-formamide / 0.33 h / 0 °C

3.2: 0 - 20 °C

3.3: 65 °C

4.1: sodium hydrogencarbonate / ethanol / 6 h / 150 °C

With dmap; sodium hydride; sodium hydrogencarbonate; triethylamine; sodium hydroxide; In tetrahydrofuran; 1,2-dimethoxyethane; ethanol; water; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2012.03.015

Reference yield:

: 89792-20-1
6-methyl-7H-pyrrolo[2,3-d]pyrimidine-2,4-diol

: 1355173-69-1
2-((2-((R)-3-aminopiperidin-1-yl)-6-methyl-4-oxo-4,7-dihydro-3H-pyrrolo[2,3-d]pyrimidin-3-yl)methyl)benzonitrile

Guidance literature:: Multi-step reaction with 5 steps

1.1: N-ethyl-N,N-diisopropylamine; trichlorophosphate / toluene / 70 - 80 °C

2.1: sodium hydroxide / water / 80 °C

2.2: pH 6

3.1: dmap; triethylamine / tetrahydrofuran / 0.5 h / 0 °C

3.2: 20 °C

4.1: sodium hydride / 1,2-dimethoxyethane; N,N-dimethyl-formamide / 0.33 h / 0 °C

4.2: 0 - 20 °C

4.3: 65 °C

5.1: sodium hydrogencarbonate / ethanol / 6 h / 150 °C

With dmap; sodium hydride; sodium hydrogencarbonate; triethylamine; N-ethyl-N,N-diisopropylamine; sodium hydroxide; trichlorophosphate; In tetrahydrofuran; 1,2-dimethoxyethane; ethanol; water; N,N-dimethyl-formamide; toluene;
DOI:10.1016/j.ejmech.2012.03.015