N-(4-chlorophenyl)-N'-(6-phenyl-4H-<1,2,4>triazolo<4,3-a><1,4>benzodiazepin-4-yl)urea

Base Information

Chemical Name:N-(4-chlorophenyl)-N'-(6-phenyl-4H-<1,2,4>triazolo<4,3-a><1,4>benzodiazepin-4-yl)urea
CAS No.:111113-21-4
Molecular Formula:C₂₃H₁₇ClN₆O
Molecular Weight:428.881
Hs Code.:

Synonyms:N-(4-chlorophenyl)-N'-(6-phenyl-4H-<1,2,4>triazolo<4,3-a><1,4>benzodiazepin-4-yl)urea

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Chemical Property of N-(4-chlorophenyl)-N'-(6-phenyl-4H-<1,2,4>triazolo<4,3-a><1,4>benzodiazepin-4-yl)urea

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Technology Process of N-(4-chlorophenyl)-N'-(6-phenyl-4H-<1,2,4>triazolo<4,3-a><1,4>benzodiazepin-4-yl)urea

There total 5 articles about N-(4-chlorophenyl)-N'-(6-phenyl-4H-<1,2,4>triazolo<4,3-a><1,4>benzodiazepin-4-yl)urea 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: 32.0%

: 104-12-1
p-chlorphenylisocyanate

: 111113-18-9
6-phenyl-4H-<1,2,4>triazolo<4,3-a><1,4>benzodiazepin-4-ylamine formate salt

: 111113-21-4
N-(4-chlorophenyl)-N'-(6-phenyl-4H-<1,2,4>triazolo<4,3-a><1,4>benzodiazepin-4-yl)urea

Guidance literature:: With triethylamine; In tetrahydrofuran;
DOI:10.1021/jm00396a028

Reference yield:

: 108895-98-3
benzyl 2-oxo-5-phenyl-2,3-dihydro-1H-benzo[e][1,4]diazepin-3-ylcarbamate

: 111113-21-4
N-(4-chlorophenyl)-N'-(6-phenyl-4H-<1,2,4>triazolo<4,3-a><1,4>benzodiazepin-4-yl)urea

Guidance literature:: Multi-step reaction with 5 steps

1: 92 percent / Lawesson's reagent / toluene / 5 h / 110 °C

2: NH₂NH₂ / methanol / 1.5 h / 23 °C

3: 65 percent / H₂SO₄ / ethanol / 10 h / 23 °C

4: 90 percent / Pd/C / methanol; H₂O / 1.5 h

5: 32 percent / Et₃N / tetrahydrofuran

With Lawessons reagent; sulfuric acid; triethylamine; hydrazine; palladium on activated charcoal; In tetrahydrofuran; methanol; ethanol; water; toluene;
DOI:10.1021/jm00396a028

Reference yield:

: 111113-10-1
phenylmethyl N-[2,3-dihydro-5-phenyl-2-thioxo-1H-1,4-benzodiazepin-3-yl]carbamate

: 111113-21-4
N-(4-chlorophenyl)-N'-(6-phenyl-4H-<1,2,4>triazolo<4,3-a><1,4>benzodiazepin-4-yl)urea

Guidance literature:: Multi-step reaction with 4 steps

1: NH₂NH₂ / methanol / 1.5 h / 23 °C

2: 65 percent / H₂SO₄ / ethanol / 10 h / 23 °C

3: 90 percent / Pd/C / methanol; H₂O / 1.5 h

4: 32 percent / Et₃N / tetrahydrofuran

With sulfuric acid; triethylamine; hydrazine; palladium on activated charcoal; In tetrahydrofuran; methanol; ethanol; water;
DOI:10.1021/jm00396a028