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C29H23BrN4O3S

Base Information Edit
  • Chemical Name:C29H23BrN4O3S
  • CAS No.:1261277-00-2
  • Molecular Formula:C29H23BrN4O3S
  • Molecular Weight:587.497
  • Hs Code.:
  • Mol file:1261277-00-2.mol
C<sub>29</sub>H<sub>23</sub>BrN<sub>4</sub>O<sub>3</sub>S

Synonyms:C29H23BrN4O3S

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Chemical Property of C29H23BrN4O3S Edit
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Technology Process of C29H23BrN4O3S

There total 11 articles about C29H23BrN4O3S 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:
Guidance literature:
4-bromopyridine-3-carboxylic acid; With oxalyl dichloride; N,N-dimethyl-formamide; at 20 ℃; for 0.0833333h;
C23H21N3O2S; With pyridine; In N,N-dimethyl-formamide; at 20 ℃; for 0.0833333h;
Guidance literature:
Multi-step reaction with 7 steps
1.1: trichlorophosphate / 5 h / 20 °C / Reflux
1.2: Cooling with ice
2.1: ethanol; sodium / 0.5 h / Cooling with ice
2.2: 3.5 h / 0 °C / Reflux
3.1: hydrogen bromide; acetic acid / Reflux
3.2: 6 h / Reflux
4.1: pyridine; HATU / 16 h / 20 °C / Inert atmosphere
5.1: pyridine / acetonitrile / 2 h / 20 °C / Inert atmosphere
6.1: hydrogenchloride; hydrogen / palladium 10% on activated carbon / ethanol; water / 2.33 h / 20 °C / Inert atmosphere
7.1: oxalyl dichloride / N,N-dimethyl-formamide / 0.08 h / 20 °C
7.2: 0.08 h / 20 °C
With pyridine; hydrogenchloride; oxalyl dichloride; ethanol; hydrogen bromide; hydrogen; sodium; acetic acid; HATU; trichlorophosphate; palladium 10% on activated carbon; N,N-dimethyl-formamide; In ethanol; water; acetonitrile;
Guidance literature:
Multi-step reaction with 9 steps
1.1: potassium carbonate / butanone, 1-
2.1: potassium tert-butylate / toluene
3.1: trichlorophosphate / 5 h / 20 °C / Reflux
3.2: Cooling with ice
4.1: ethanol; sodium / 0.5 h / Cooling with ice
4.2: 3.5 h / 0 °C / Reflux
5.1: hydrogen bromide; acetic acid / Reflux
5.2: 6 h / Reflux
6.1: pyridine; HATU / 16 h / 20 °C / Inert atmosphere
7.1: pyridine / acetonitrile / 2 h / 20 °C / Inert atmosphere
8.1: hydrogenchloride; hydrogen / palladium 10% on activated carbon / ethanol; water / 2.33 h / 20 °C / Inert atmosphere
9.1: oxalyl dichloride / N,N-dimethyl-formamide / 0.08 h / 20 °C
9.2: 0.08 h / 20 °C
With pyridine; hydrogenchloride; oxalyl dichloride; ethanol; potassium tert-butylate; hydrogen bromide; hydrogen; sodium; potassium carbonate; acetic acid; HATU; trichlorophosphate; palladium 10% on activated carbon; N,N-dimethyl-formamide; In ethanol; butanone, 1-; water; toluene; acetonitrile;
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