5-[3-(3-bromo-phenyl)-propyl]-6-iodo-pyrimidin-4-ylamine

Base Information

Chemical Name:5-[3-(3-bromo-phenyl)-propyl]-6-iodo-pyrimidin-4-ylamine
CAS No.:454685-49-5
Molecular Formula:C₁₃H₁₃BrIN₃
Molecular Weight:418.075
Hs Code.:

Synonyms:5-[3-(3-bromo-phenyl)-propyl]-6-iodo-pyrimidin-4-ylamine

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Chemical Property of 5-[3-(3-bromo-phenyl)-propyl]-6-iodo-pyrimidin-4-ylamine

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Technology Process of 5-[3-(3-bromo-phenyl)-propyl]-6-iodo-pyrimidin-4-ylamine

There total 6 articles about 5-[3-(3-bromo-phenyl)-propyl]-6-iodo-pyrimidin-4-ylamine 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:

: 16019-30-0
5-(prop-2-en-1-yl)pyrimidine-4,6-diol

: 454685-49-5
5-[3-(3-bromo-phenyl)-propyl]-6-iodo-pyrimidin-4-ylamine

Guidance literature:: Multi-step reaction with 5 steps

1: POCl₃ / Heating

2: 88 percent / NH₃ / ethanol / 16 h / 100 °C

3: diisopropylethylamine; tri-o-tolylphosphine; Pd(PPh₃A)4 / dioxane / Heating

4: H₂ / 5 percent Pt/C / methanol; ethyl acetate / 3040 Torr

5: 40 percent HI; NaI / 70 °C

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; ammonia; hydrogen iodide; hydrogen; N-ethyl-N,N-diisopropylamine; tris-(o-tolyl)phosphine; sodium iodide; trichlorophosphate; platinum on activated charcoal; In 1,4-dioxane; methanol; ethanol; ethyl acetate;
DOI:10.1021/jm020049a

Reference yield:

: 2049-80-1
(2-propenyl)propanedioic acid diethyl ester

: 454685-49-5
5-[3-(3-bromo-phenyl)-propyl]-6-iodo-pyrimidin-4-ylamine

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium ethoxide / ethanol / 0 °C

1.2: ethanol / 20 °C

2.1: POCl₃ / Heating

3.1: 88 percent / NH₃ / ethanol / 16 h / 100 °C

4.1: diisopropylethylamine; tri-o-tolylphosphine; Pd(PPh₃A)4 / dioxane / Heating

5.1: H₂ / 5 percent Pt/C / methanol; ethyl acetate / 3040 Torr

6.1: 40 percent HI; NaI / 70 °C

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; ammonia; hydrogen iodide; hydrogen; sodium ethanolate; N-ethyl-N,N-diisopropylamine; tris-(o-tolyl)phosphine; sodium iodide; trichlorophosphate; platinum on activated charcoal; In 1,4-dioxane; methanol; ethanol; ethyl acetate;
DOI:10.1021/jm020049a

Reference yield:

: 16019-31-1
5-allyl-4,6-dichloropyrimidine

: 454685-49-5
5-[3-(3-bromo-phenyl)-propyl]-6-iodo-pyrimidin-4-ylamine

Guidance literature:: Multi-step reaction with 4 steps

1: 88 percent / NH₃ / ethanol / 16 h / 100 °C

2: diisopropylethylamine; tri-o-tolylphosphine; Pd(PPh₃A)4 / dioxane / Heating

3: H₂ / 5 percent Pt/C / methanol; ethyl acetate / 3040 Torr

4: 40 percent HI; NaI / 70 °C

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; ammonia; hydrogen iodide; hydrogen; N-ethyl-N,N-diisopropylamine; tris-(o-tolyl)phosphine; sodium iodide; platinum on activated charcoal; In 1,4-dioxane; methanol; ethanol; ethyl acetate;
DOI:10.1021/jm020049a