Carbamic acid, [3-[[4-amino-6-(4-morpholinyl)-1,3,5-triazin-2-yl]oxy]-2,2-bis[[4-(decyloxy )phenyl]methyl]propyl]-, 1,1-dimethylethyl ester

Base Information

Chemical Name:Carbamic acid, [3-[[4-amino-6-(4-morpholinyl)-1,3,5-triazin-2-yl]oxy]-2,2-bis[[4-(decyloxy )phenyl]methyl]propyl]-, 1,1-dimethylethyl ester
CAS No.:437613-35-9
Molecular Formula:C49H78N6O6
Molecular Weight:847.195
Hs Code.:
Mol file:437613-35-9.mol

Synonyms:

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Chemical Property of Carbamic acid, [3-[[4-amino-6-(4-morpholinyl)-1,3,5-triazin-2-yl]oxy]-2,2-bis[[4-(decyloxy )phenyl]methyl]propyl]-, 1,1-dimethylethyl ester

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MSDS Files:: SDS file from LookChem

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Technology Process of Carbamic acid, [3-[[4-amino-6-(4-morpholinyl)-1,3,5-triazin-2-yl]oxy]-2,2-bis[[4-(decyloxy )phenyl]methyl]propyl]-, 1,1-dimethylethyl ester

There total 6 articles about Carbamic acid, [3-[[4-amino-6-(4-morpholinyl)-1,3,5-triazin-2-yl]oxy]-2,2-bis[[4-(decyloxy )phenyl]methyl]propyl]-, 1,1-dimethylethyl ester 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: 94.0%

: 110-91-8,99108-56-2
morpholine

: 437613-34-8
[3-(4-amino-6-chloro-[1,3,5]triazin-2-yloxy)-2,2-bis-(4-decyloxy-benzyl)-propyl]-carbamic acid tert-butyl ester

: 437613-35-9
[3-(4-amino-6-morpholin-4-yl-[1,3,5]triazin-2-yloxy)-2,2-bis-(4-decyloxy-benzyl)-propyl]-carbamic acid tert-butyl ester

Guidance literature:: In chloroform; for 1h; Heating;
DOI:10.1021/ja012696h

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 437613-35-9
[3-(4-amino-6-morpholin-4-yl-[1,3,5]triazin-2-yloxy)-2,2-bis-(4-decyloxy-benzyl)-propyl]-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 91 percent / CH₂Cl₂ / 16 h / 20 °C

2: 2,6-lutidine / toluene / 16 h / 80 °C

3: 29.6 g / NH₃ / propan-2-ol; CH₂Cl₂ / 3 h

4: 94 percent / CHCl₃ / 1 h / Heating

With 2,6-dimethylpyridine; ammonia; In dichloromethane; chloroform; isopropyl alcohol; toluene;
DOI:10.1021/ja012696h

Reference yield:

: 110482-74-1
1-chloromethyl-4-decyloxybenzene

: 437613-35-9
[3-(4-amino-6-morpholin-4-yl-[1,3,5]triazin-2-yloxy)-2,2-bis-(4-decyloxy-benzyl)-propyl]-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 92 percent / DBU / dimethylformamide / 1 h / 80 °C

2: 97 percent / LiAlH₄ / tetrahydrofuran / 14 h / Heating

3: 91 percent / CH₂Cl₂ / 16 h / 20 °C

4: 2,6-lutidine / toluene / 16 h / 80 °C

5: 29.6 g / NH₃ / propan-2-ol; CH₂Cl₂ / 3 h

6: 94 percent / CHCl₃ / 1 h / Heating

With 2,6-dimethylpyridine; lithium aluminium tetrahydride; ammonia; 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; dichloromethane; chloroform; N,N-dimethyl-formamide; isopropyl alcohol; toluene;
DOI:10.1021/ja012696h