1-tert-butyl-4,4-diphenyl-2-<(2-nitrophenyl)thio>-1,3-diazabuta-1,3-diene

Base Information

Chemical Name:1-tert-butyl-4,4-diphenyl-2-<(2-nitrophenyl)thio>-1,3-diazabuta-1,3-diene
CAS No.:124512-06-7
Molecular Formula:C₂₄H₂₃N₃O₂S
Molecular Weight:417.532
Hs Code.:

Synonyms:1-tert-butyl-4,4-diphenyl-2-<(2-nitrophenyl)thio>-1,3-diazabuta-1,3-diene

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Chemical Property of 1-tert-butyl-4,4-diphenyl-2-<(2-nitrophenyl)thio>-1,3-diazabuta-1,3-diene

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Technology Process of 1-tert-butyl-4,4-diphenyl-2-<(2-nitrophenyl)thio>-1,3-diazabuta-1,3-diene

There total 3 articles about 1-tert-butyl-4,4-diphenyl-2-<(2-nitrophenyl)thio>-1,3-diazabuta-1,3-diene 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: 90.0%

: 1013-88-3
Benzophenone imine

: 124512-05-6
C₁₁H₁₃ClN₂O₂S

: 124512-06-7
1-tert-butyl-4,4-diphenyl-2-<(2-nitrophenyl)thio>-1,3-diazabuta-1,3-diene

Guidance literature:: With triethylamine; In tetrahydrofuran; for 6h; Ambient temperature;
DOI:10.1021/jo00293a011

Reference yield:

: 119072-55-8,7188-38-7
tert-butylisonitrile

: 124512-06-7
1-tert-butyl-4,4-diphenyl-2-<(2-nitrophenyl)thio>-1,3-diazabuta-1,3-diene

Guidance literature:: Multi-step reaction with 2 steps

1: tetrahydrofuran

2: 90 percent / NEt₃ / tetrahydrofuran / 6 h / Ambient temperature

With triethylamine; In tetrahydrofuran;
DOI:10.1021/jo00293a011

Reference yield:

: 7669-54-7
2-nitrobenzenesulfenyl chloride

: 124512-06-7
1-tert-butyl-4,4-diphenyl-2-<(2-nitrophenyl)thio>-1,3-diazabuta-1,3-diene

Guidance literature:: Multi-step reaction with 2 steps

1: tetrahydrofuran

2: 90 percent / NEt₃ / tetrahydrofuran / 6 h / Ambient temperature

With triethylamine; In tetrahydrofuran;
DOI:10.1021/jo00293a011