2-(3,4-dichlorophenyl)-N-{4-[(7-isopropyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)carbonyl]pyridin-2-yl}acetamide

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Chemical Name:2-(3,4-dichlorophenyl)-N-{4-[(7-isopropyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)carbonyl]pyridin-2-yl}acetamide
CAS No.:1596335-57-7
Molecular Formula:C₂₃H₁₉Cl₂N₅O₂
Molecular Weight:468.342
Hs Code.:

Synonyms:2-(3,4-dichlorophenyl)-N-{4-[(7-isopropyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)carbonyl]pyridin-2-yl}acetamide

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Chemical Property of 2-(3,4-dichlorophenyl)-N-{4-[(7-isopropyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)carbonyl]pyridin-2-yl}acetamide

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Technology Process of 2-(3,4-dichlorophenyl)-N-{4-[(7-isopropyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)carbonyl]pyridin-2-yl}acetamide

There total 4 articles about 2-(3,4-dichlorophenyl)-N-{4-[(7-isopropyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)carbonyl]pyridin-2-yl}acetamide 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: 15.0%

: 5807-30-7
3,4-dichlorophenyl acetic acid

: 1596336-90-1
(2-aminopyridin-4-yl)-(7-isopropyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)methanone

: 1596335-57-7
2-(3,4-dichlorophenyl)-N-{4-[(7-isopropyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)carbonyl]pyridin-2-yl}acetamide

Guidance literature:: With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; at 25 ℃; for 16h;

Reference yield:

: 5-iodo-7-isopropyl-7H-pyrrolo[2,3-d]pyrimidine

: 1596335-57-7
2-(3,4-dichlorophenyl)-N-{4-[(7-isopropyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)carbonyl]pyridin-2-yl}acetamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: isopropylmagnesium chloride / tetrahydrofuran / 0.5 h / 0 °C

1.2: 18 h / 0 - 20 °C

2.1: ammonium hydroxide; copper(ll) sulfate pentahydrate / 16 h / 140 °C / Sealed tube

3.1: N-ethyl-N,N-diisopropylamine; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide / tetrahydrofuran / 16 h / 25 °C

With ammonium hydroxide; copper(ll) sulfate pentahydrate; isopropylmagnesium chloride; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran;

Reference yield:

: 175791-53-4
5-Iodopyrrolo<2,3-d>pyrimidine

: 1596335-57-7
2-(3,4-dichlorophenyl)-N-{4-[(7-isopropyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)carbonyl]pyridin-2-yl}acetamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: caesium carbonate / N,N-dimethyl-formamide / 3 h / 20 °C

2.1: isopropylmagnesium chloride / tetrahydrofuran / 0.5 h / 0 °C

2.2: 18 h / 0 - 20 °C

3.1: ammonium hydroxide; copper(ll) sulfate pentahydrate / 16 h / 140 °C / Sealed tube

4.1: N-ethyl-N,N-diisopropylamine; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide / tetrahydrofuran / 16 h / 25 °C

With ammonium hydroxide; copper(ll) sulfate pentahydrate; isopropylmagnesium chloride; caesium carbonate; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; N,N-dimethyl-formamide;