5-tert-butyl 1-isopropyl 5-benzyl-1H-1,2,4-triazole-1,5(2H,5H)-dicarboxylate

Base Information

Chemical Name:5-tert-butyl 1-isopropyl 5-benzyl-1H-1,2,4-triazole-1,5(2H,5H)-dicarboxylate
CAS No.:1261037-36-8
Molecular Formula:C₁₈H₂₅N₃O₄
Molecular Weight:347.414
Hs Code.:

Synonyms:5-tert-butyl 1-isopropyl 5-benzyl-1H-1,2,4-triazole-1,5(2H,5H)-dicarboxylate

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Chemical Property of 5-tert-butyl 1-isopropyl 5-benzyl-1H-1,2,4-triazole-1,5(2H,5H)-dicarboxylate

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Technology Process of 5-tert-butyl 1-isopropyl 5-benzyl-1H-1,2,4-triazole-1,5(2H,5H)-dicarboxylate

There total 4 articles about 5-tert-butyl 1-isopropyl 5-benzyl-1H-1,2,4-triazole-1,5(2H,5H)-dicarboxylate 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: 40.0%

: 1261037-18-6
3-tert-butyl 1,2-diisopropyl 3-benzyl-1H-1,2,4-triazole-1,2,3(3H)-tricarboxylate

: 1261037-36-8
5-tert-butyl 1-isopropyl 5-benzyl-1H-1,2,4-triazole-1,5(2H,5H)-dicarboxylate

Guidance literature:: With ethanol; sodium ethanolate; In chloroform; at 50 ℃; for 48h;
DOI:10.1021/ol102812c

Reference yield:

: 16367-71-8
t-butyl (RS)-phenylalaninate

: 1261037-36-8
5-tert-butyl 1-isopropyl 5-benzyl-1H-1,2,4-triazole-1,5(2H,5H)-dicarboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: acetic anhydride / 2 h / 0 - 20 °C

2: triethylamine; trichlorophosphate / tetrahydrofuran / 1 h / -78 - 0 °C

3: 1,8-diazabicyclo[5.4.0]undec-7-ene / acetonitrile / 25 h / 20 °C

4: ethanol; sodium ethanolate / chloroform / 48 h / 50 °C

With ethanol; sodium ethanolate; acetic anhydride; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; trichlorophosphate; In tetrahydrofuran; chloroform; acetonitrile;
DOI:10.1021/ol102812c

Reference yield:

: 61900-41-2
N-Formylphenylalanin-tert-butylester

: 1261037-36-8
5-tert-butyl 1-isopropyl 5-benzyl-1H-1,2,4-triazole-1,5(2H,5H)-dicarboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine; trichlorophosphate / tetrahydrofuran / 1 h / -78 - 0 °C

2: 1,8-diazabicyclo[5.4.0]undec-7-ene / acetonitrile / 25 h / 20 °C

3: ethanol; sodium ethanolate / chloroform / 48 h / 50 °C

With ethanol; sodium ethanolate; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; trichlorophosphate; In tetrahydrofuran; chloroform; acetonitrile;
DOI:10.1021/ol102812c