2-(trans-4-(3-bromo-6-(2,5-dimethyl-1H-pyrrol-1-yl)-2-methylpyridin-4-ylamino)cyclohexyloxy)ethanol

Base Information

Chemical Name:2-(trans-4-(3-bromo-6-(2,5-dimethyl-1H-pyrrol-1-yl)-2-methylpyridin-4-ylamino)cyclohexyloxy)ethanol
CAS No.:1552300-17-0
Molecular Formula:C₂₀H₂₈BrN₃O₂
Molecular Weight:422.365
Hs Code.:

Synonyms:2-(trans-4-(3-bromo-6-(2,5-dimethyl-1H-pyrrol-1-yl)-2-methylpyridin-4-ylamino)cyclohexyloxy)ethanol

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Chemical Property of 2-(trans-4-(3-bromo-6-(2,5-dimethyl-1H-pyrrol-1-yl)-2-methylpyridin-4-ylamino)cyclohexyloxy)ethanol

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Technology Process of 2-(trans-4-(3-bromo-6-(2,5-dimethyl-1H-pyrrol-1-yl)-2-methylpyridin-4-ylamino)cyclohexyloxy)ethanol

There total 4 articles about 2-(trans-4-(3-bromo-6-(2,5-dimethyl-1H-pyrrol-1-yl)-2-methylpyridin-4-ylamino)cyclohexyloxy)ethanol 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: 36.0%

: 1072-53-3
ethyleneglycol sulfate

: 1552300-16-9
trans-4-(3-bromo-6-(2,5-dimethyl-1H-pyrrol-1-yl)-2-methylpyridin-4-ylamino)cyclohexanol

: 1552300-17-0
2-(trans-4-(3-bromo-6-(2,5-dimethyl-1H-pyrrol-1-yl)-2-methylpyridin-4-ylamino)cyclohexyloxy)ethanol

Guidance literature:: trans-4-(3-bromo-6-(2,5-dimethyl-1H-pyrrol-1-yl)-2-methylpyridin-4-ylamino)cyclohexanol; With sodium hydride; In mineral oil; at 0 ℃; for 2.5h;

ethyleneglycol sulfate; In mineral oil; at 0 ℃;

With toluene-4-sulfonic acid; In 1,4-dioxane; water; at 40 ℃; for 3h;
DOI:10.1016/j.bmcl.2013.12.112

Reference yield:

: 1541125-83-0
3-bromo-6-(2,5-dimethyl-1H-pyrrol-1-yl)-2-methylpyridine

: 1552300-17-0
2-(trans-4-(3-bromo-6-(2,5-dimethyl-1H-pyrrol-1-yl)-2-methylpyridin-4-ylamino)cyclohexyloxy)ethanol

Guidance literature:: Multi-step reaction with 3 steps

1.1: diisopropylamine; n-butyllithium / tetrahydrofuran; hexane / 0.5 h / -78 - -30 °C / Inert atmosphere

1.2: 0.5 h / -78 °C / Inert atmosphere

2.1: N-ethyl-N,N-diisopropylamine; 1-methyl-pyrrolidin-2-one / 24 h / 160 °C / Sealed tube

3.1: sodium hydride / mineral oil / 2.5 h / 0 °C

3.2: 0 °C

3.3: 3 h / 40 °C

With 1-methyl-pyrrolidin-2-one; n-butyllithium; sodium hydride; diisopropylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; hexane; mineral oil;
DOI:10.1016/j.bmcl.2013.12.112

Reference yield:

: 1552300-15-8
3-bromo-6-(2,5-dimethyl-1H-pyrrol-1-yl)-4-iodo-2-methylpyridine

: 1552300-17-0
2-(trans-4-(3-bromo-6-(2,5-dimethyl-1H-pyrrol-1-yl)-2-methylpyridin-4-ylamino)cyclohexyloxy)ethanol

Guidance literature:: Multi-step reaction with 2 steps

1.1: N-ethyl-N,N-diisopropylamine; 1-methyl-pyrrolidin-2-one / 24 h / 160 °C / Sealed tube

2.1: sodium hydride / mineral oil / 2.5 h / 0 °C

2.2: 0 °C

2.3: 3 h / 40 °C

With 1-methyl-pyrrolidin-2-one; sodium hydride; N-ethyl-N,N-diisopropylamine; In mineral oil;
DOI:10.1016/j.bmcl.2013.12.112