(Z)-6-amino-2-bromo-3-(4-chloro-5H-1,2,3-dithiazol-5-ylideneamino)benzonitrile

Base Information

Chemical Name:(Z)-6-amino-2-bromo-3-(4-chloro-5H-1,2,3-dithiazol-5-ylideneamino)benzonitrile
CAS No.:1425945-84-1
Molecular Formula:C₉H₄BrClN₄S₂
Molecular Weight:347.647
Hs Code.:

Synonyms:(Z)-6-amino-2-bromo-3-(4-chloro-5H-1,2,3-dithiazol-5-ylideneamino)benzonitrile

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Chemical Property of (Z)-6-amino-2-bromo-3-(4-chloro-5H-1,2,3-dithiazol-5-ylideneamino)benzonitrile

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Technology Process of (Z)-6-amino-2-bromo-3-(4-chloro-5H-1,2,3-dithiazol-5-ylideneamino)benzonitrile

There total 5 articles about (Z)-6-amino-2-bromo-3-(4-chloro-5H-1,2,3-dithiazol-5-ylideneamino)benzonitrile 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: 100.0%

: 1425945-83-0
(Z)-tert-butyl-3-bromo-4-(4-chloro-5H-1,2,3-dithiazol-5-ylideneamino)-2-cyanophenylcarbamate

: 1425945-84-1
(Z)-6-amino-2-bromo-3-(4-chloro-5H-1,2,3-dithiazol-5-ylideneamino)benzonitrile

Guidance literature:: With acetic acid; at 118 ℃; for 2h; Microwave irradiation;

Reference yield:

: 17420-30-3
5-nitroanthranilonitrile

: 1425945-84-1
(Z)-6-amino-2-bromo-3-(4-chloro-5H-1,2,3-dithiazol-5-ylideneamino)benzonitrile

Guidance literature:: Multi-step reaction with 5 steps

1.1: dmap; triethylamine / dichloromethane / 4 h / 20 °C / Inert atmosphere

2.1: palladium 10% on activated carbon; ammonium formate / ethanol / 0.5 h / 85 °C / Microwave irradiation

3.1: bromine; acetic acid / dichloromethane / 2.5 h / 20 °C / Inert atmosphere

4.1: dichloromethane / 3 h / 20 °C / Inert atmosphere

4.2: 1 h / 20 °C

5.1: acetic acid / 2 h / 118 °C / Microwave irradiation

With dmap; palladium 10% on activated carbon; bromine; ammonium formate; acetic acid; triethylamine; In ethanol; dichloromethane;

Reference yield:

: 1425945-82-9
tert-butyl 4-amino-3-bromo-2-cyanophenylcarbamate

: 1425945-84-1
(Z)-6-amino-2-bromo-3-(4-chloro-5H-1,2,3-dithiazol-5-ylideneamino)benzonitrile

Guidance literature:: Multi-step reaction with 2 steps

1.1: dichloromethane / 3 h / 20 °C / Inert atmosphere

1.2: 1 h / 20 °C

2.1: acetic acid / 2 h / 118 °C / Microwave irradiation

With acetic acid; In dichloromethane;