methyl 2-(2-(3-bromophenyl)-7-iodo-5-methylpyrazolo[1,5-a]pyrimidin-6-yl)-2-hydroxyacetate

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Chemical Name:methyl 2-(2-(3-bromophenyl)-7-iodo-5-methylpyrazolo[1,5-a]pyrimidin-6-yl)-2-hydroxyacetate
CAS No.:1567213-44-8
Molecular Formula:C₁₆H₁₃BrIN₃O₃
Molecular Weight:502.106
Hs Code.:

Synonyms:methyl 2-(2-(3-bromophenyl)-7-iodo-5-methylpyrazolo[1,5-a]pyrimidin-6-yl)-2-hydroxyacetate

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Chemical Property of methyl 2-(2-(3-bromophenyl)-7-iodo-5-methylpyrazolo[1,5-a]pyrimidin-6-yl)-2-hydroxyacetate

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Technology Process of methyl 2-(2-(3-bromophenyl)-7-iodo-5-methylpyrazolo[1,5-a]pyrimidin-6-yl)-2-hydroxyacetate

There total 6 articles about methyl 2-(2-(3-bromophenyl)-7-iodo-5-methylpyrazolo[1,5-a]pyrimidin-6-yl)-2-hydroxyacetate 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: 67.6%

: 1567213-41-5
methyl 2-(2-(3-bromophenyl)-7-iodo-5-methylpyrazolo[1,5-a]pyrimidin-6-yl)acetate

: 1567213-44-8
methyl 2-(2-(3-bromophenyl)-7-iodo-5-methylpyrazolo[1,5-a]pyrimidin-6-yl)-2-hydroxyacetate

Guidance literature:: methyl 2-(2-(3-bromophenyl)-7-iodo-5-methylpyrazolo[1,5-a]pyrimidin-6-yl)acetate; With potassium hexamethylsilazane; In tetrahydrofuran; at -78 ℃; for 0.583333h;

With N-(benzenesulfonyl)-3-phenyloxaziridine; In tetrahydrofuran; at -78 ℃; for 0.5h;

Reference yield:

: 1567213-35-7
methyl 2-(2-(3-bromophenyl)-7-hydroxy-5-methylpyrazolo[1,5-a]pyrimidin-6-yl)acetate

: 1567213-44-8
methyl 2-(2-(3-bromophenyl)-7-iodo-5-methylpyrazolo[1,5-a]pyrimidin-6-yl)-2-hydroxyacetate

Guidance literature:: Multi-step reaction with 3 steps

1.1: N,N-dimethyl-aniline; trichlorophosphate / 2.5 h / 120 °C

2.1: sodium iodide / acetonitrile / 5 h / 80 °C

3.1: potassium hexamethylsilazane / tetrahydrofuran / 0.58 h / -78 °C

3.2: 0.5 h / -78 °C

With potassium hexamethylsilazane; N,N-dimethyl-aniline; sodium iodide; trichlorophosphate; In tetrahydrofuran; acetonitrile; 3.1: |Davis' Oxaziridine Oxidations / 3.2: |Davis' Oxaziridine Oxidations;

Reference yield:

: 1567213-38-0
methyl 2-(2-(3-bromophenyl)-7-chloro-5-methylpyrazolo[1,5-a]pyrimidin-6-yl)acetate

: 1567213-44-8
methyl 2-(2-(3-bromophenyl)-7-iodo-5-methylpyrazolo[1,5-a]pyrimidin-6-yl)-2-hydroxyacetate

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium iodide / acetonitrile / 5 h / 80 °C

2.1: potassium hexamethylsilazane / tetrahydrofuran / 0.58 h / -78 °C

2.2: 0.5 h / -78 °C

With potassium hexamethylsilazane; sodium iodide; In tetrahydrofuran; acetonitrile; 2.1: |Davis' Oxaziridine Oxidations / 2.2: |Davis' Oxaziridine Oxidations;