(2-aminopyridin-4-yl)-[7-(trans-4-{[tert-butyl(dimethyl)silyl]oxy}cyclohexyl)-7H-pyrrolo[2,3-d]pyrimidin-5-yl]methanone

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Chemical Name:(2-aminopyridin-4-yl)-[7-(trans-4-{[tert-butyl(dimethyl)silyl]oxy}cyclohexyl)-7H-pyrrolo[2,3-d]pyrimidin-5-yl]methanone
CAS No.:1596336-74-1
Molecular Formula:C₂₄H₃₃N₅O₂Si
Molecular Weight:451.644
Hs Code.:

Synonyms:(2-aminopyridin-4-yl)-[7-(trans-4-{[tert-butyl(dimethyl)silyl]oxy}cyclohexyl)-7H-pyrrolo[2,3-d]pyrimidin-5-yl]methanone

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Chemical Property of (2-aminopyridin-4-yl)-[7-(trans-4-{[tert-butyl(dimethyl)silyl]oxy}cyclohexyl)-7H-pyrrolo[2,3-d]pyrimidin-5-yl]methanone

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Technology Process of (2-aminopyridin-4-yl)-[7-(trans-4-{[tert-butyl(dimethyl)silyl]oxy}cyclohexyl)-7H-pyrrolo[2,3-d]pyrimidin-5-yl]methanone

There total 9 articles about (2-aminopyridin-4-yl)-[7-(trans-4-{[tert-butyl(dimethyl)silyl]oxy}cyclohexyl)-7H-pyrrolo[2,3-d]pyrimidin-5-yl]methanone 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:

: 1595292-44-6
2-[(diphenylmethylene)amino]-N-methoxy-N-methylisonicotinamide

: 1596336-74-1
(2-aminopyridin-4-yl)-[7-(trans-4-{[tert-butyl(dimethyl)silyl]oxy}cyclohexyl)-7H-pyrrolo[2,3-d]pyrimidin-5-yl]methanone

Guidance literature:: Multi-step reaction with 2 steps

1.1: isopropylmagnesium chloride / tetrahydrofuran / 1 h / 0 °C

1.2: 16 h / 0 - 20 °C

2.1: citric acid / tetrahydrofuran / 2 h / 20 °C

With isopropylmagnesium chloride; citric acid; In tetrahydrofuran;

Reference yield:

: 656257-69-1
2-bromo-N-methyl-N-(methyloxy)-4-pyridinecarboxamide

: 1596336-74-1
(2-aminopyridin-4-yl)-[7-(trans-4-{[tert-butyl(dimethyl)silyl]oxy}cyclohexyl)-7H-pyrrolo[2,3-d]pyrimidin-5-yl]methanone

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium t-butanolate; tert-butyl XPhos; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / toluene / 2 h / 20 °C

2.1: isopropylmagnesium chloride / tetrahydrofuran / 1 h / 0 °C

2.2: 16 h / 0 - 20 °C

3.1: citric acid / tetrahydrofuran / 2 h / 20 °C

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; isopropylmagnesium chloride; citric acid; sodium t-butanolate; tert-butyl XPhos; In tetrahydrofuran; toluene;

Reference yield:

: 1596337-22-2
7-(trans-4-{[tert-butyl(dimethyl)silyl]oxy}cyclohexyl)-5-iodo-7H-pyrrolo[2,3-d]pyrimidine

: 1596336-74-1
(2-aminopyridin-4-yl)-[7-(trans-4-{[tert-butyl(dimethyl)silyl]oxy}cyclohexyl)-7H-pyrrolo[2,3-d]pyrimidin-5-yl]methanone

Guidance literature:: Multi-step reaction with 2 steps

1.1: isopropylmagnesium chloride / tetrahydrofuran / 1 h / 0 °C

1.2: 16 h / 0 - 20 °C

2.1: citric acid / tetrahydrofuran / 2 h / 20 °C

With isopropylmagnesium chloride; citric acid; In tetrahydrofuran;