7,8-dichloro-1-(4-nitrophenyl)-3,5-dihydro-4H-2,3-benzodiazepin-4-thione

Base Information

Chemical Name:7,8-dichloro-1-(4-nitrophenyl)-3,5-dihydro-4H-2,3-benzodiazepin-4-thione
CAS No.:220445-10-3
Molecular Formula:C₁₅H₉Cl₂N₃O₂S
Molecular Weight:366.227
Hs Code.:

Synonyms:7,8-dichloro-1-(4-nitrophenyl)-3,5-dihydro-4H-2,3-benzodiazepin-4-thione

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Chemical Property of 7,8-dichloro-1-(4-nitrophenyl)-3,5-dihydro-4H-2,3-benzodiazepin-4-thione

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Technology Process of 7,8-dichloro-1-(4-nitrophenyl)-3,5-dihydro-4H-2,3-benzodiazepin-4-thione

There total 5 articles about 7,8-dichloro-1-(4-nitrophenyl)-3,5-dihydro-4H-2,3-benzodiazepin-4-thione 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: 61.0%

: 220445-15-8
7,8-dichloro-1-(4-nitrophenyl)-3,5-dihydro-4H-2,3-benzodiazepin-4-one

: 220445-10-3
7,8-dichloro-1-(4-nitrophenyl)-3,5-dihydro-4H-2,3-benzodiazepin-4-thione

Guidance literature:: With tetraphosphorus decasulfide; In pyridine; at 80 ℃;
DOI:10.1016/S0968-0896(00)00133-4

Reference yield:

: 555-16-8
4-nitrobenzaldehdye

: 220445-10-3
7,8-dichloro-1-(4-nitrophenyl)-3,5-dihydro-4H-2,3-benzodiazepin-4-thione

Guidance literature:: Multi-step reaction with 4 steps

1.1: 30 percent / ZnCl₂; HCl / benzene

2.1: 54 percent / CrO₃; H₂SO₄ / acetone / 16 h

3.1: NH₂NH₂*H₂O / propan-2-ol / 6 h / Heating

3.2: 73 percent / DCC / CH₂Cl₂ / 20 °C

4.1: 61 percent / P₂S₅ / pyridine / 80 °C

With chromium(VI) oxide; hydrogenchloride; tetraphosphorus decasulfide; sulfuric acid; hydrazine hydrate; zinc(II) chloride; In pyridine; isopropyl alcohol; acetone; benzene; 1.1: Condensation / 2.1: Oxidation / 3.1: Condensation / 3.2: Cyclization / 4.1: Substitution;
DOI:10.1016/S0968-0896(00)00133-4

Reference yield:

: 220445-13-6
6,7-dichloro-1-(4-nitrophenyl)isochromane

: 220445-10-3
7,8-dichloro-1-(4-nitrophenyl)-3,5-dihydro-4H-2,3-benzodiazepin-4-thione

Guidance literature:: Multi-step reaction with 3 steps

1.1: 54 percent / CrO₃; H₂SO₄ / acetone / 16 h

2.1: NH₂NH₂*H₂O / propan-2-ol / 6 h / Heating

2.2: 73 percent / DCC / CH₂Cl₂ / 20 °C

3.1: 61 percent / P₂S₅ / pyridine / 80 °C

With chromium(VI) oxide; tetraphosphorus decasulfide; sulfuric acid; hydrazine hydrate; In pyridine; isopropyl alcohol; acetone; 1.1: Oxidation / 2.1: Condensation / 2.2: Cyclization / 3.1: Substitution;
DOI:10.1016/S0968-0896(00)00133-4