(3S)-3-({2-amino-5-[4-(benzyloxy)-2-methoxybenzyl]-6-methylpyrimidin-4-yl}amino)-hexan-1-ol

Base Information

Chemical Name:(3S)-3-({2-amino-5-[4-(benzyloxy)-2-methoxybenzyl]-6-methylpyrimidin-4-yl}amino)-hexan-1-ol
CAS No.:1376514-59-8
Molecular Formula:C₂₆H₃₄N₄O₃
Molecular Weight:450.581
Hs Code.:

Synonyms:(3S)-3-({2-amino-5-[4-(benzyloxy)-2-methoxybenzyl]-6-methylpyrimidin-4-yl}amino)-hexan-1-ol

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Chemical Property of (3S)-3-({2-amino-5-[4-(benzyloxy)-2-methoxybenzyl]-6-methylpyrimidin-4-yl}amino)-hexan-1-ol

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Technology Process of (3S)-3-({2-amino-5-[4-(benzyloxy)-2-methoxybenzyl]-6-methylpyrimidin-4-yl}amino)-hexan-1-ol

There total 5 articles about (3S)-3-({2-amino-5-[4-(benzyloxy)-2-methoxybenzyl]-6-methylpyrimidin-4-yl}amino)-hexan-1-ol 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: 53.0%

: 1376514-57-6
2-amino-5-[4-(benzyloxy)-2-methoxybenzyl]-6-methylpyrimidin-4-yl 2,4,6-triisopropylbenzenesulfonate

: 64197-80-4
(S)-(+)-3-amino-1-hexanol

: 1376514-59-8
(3S)-3-({2-amino-5-[4-(benzyloxy)-2-methoxybenzyl]-6-methylpyrimidin-4-yl}amino)-hexan-1-ol

Guidance literature:: With trifluoroacetic acid; In propyl cyanide; at 120 ℃; for 20h;

Reference yield:

: 171768-67-5
4-benzyloxy-1-bromo-2-methoxybenzene

: 1376514-59-8
(3S)-3-({2-amino-5-[4-(benzyloxy)-2-methoxybenzyl]-6-methylpyrimidin-4-yl}amino)-hexan-1-ol

Guidance literature:: Multi-step reaction with 4 steps

1: tetrabutyl-ammonium chloride; N-Methyldicyclohexylamine / dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II) / N,N-dimethyl-formamide / 18 h / 100 °C / Inert atmosphere

2: methanol / 5 h / 60 °C

3: 1,4-diaza-bicyclo[2.2.2]octane / tetrahydrofuran / 3 h / 50 °C

4: trifluoroacetic acid / propyl cyanide / 20 h / 120 °C

With 1,4-diaza-bicyclo[2.2.2]octane; N-Methyldicyclohexylamine; tetrabutyl-ammonium chloride; trifluoroacetic acid; dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II); In tetrahydrofuran; methanol; propyl cyanide; N,N-dimethyl-formamide; 1: Heck Reaction;

Reference yield:

: 1376514-55-4
2-amino-5-[4-(benzyloxy)-2-methoxybenzyl]-6-methylpyrimidin-4-ol

: 1376514-59-8
(3S)-3-({2-amino-5-[4-(benzyloxy)-2-methoxybenzyl]-6-methylpyrimidin-4-yl}amino)-hexan-1-ol

Guidance literature:: Multi-step reaction with 2 steps

1: 1,4-diaza-bicyclo[2.2.2]octane / tetrahydrofuran / 3 h / 50 °C

2: trifluoroacetic acid / propyl cyanide / 20 h / 120 °C

With 1,4-diaza-bicyclo[2.2.2]octane; trifluoroacetic acid; In tetrahydrofuran; propyl cyanide;