8-Chloro-6-phenyl-1-pyrrolidin-1-ylmethyl-4H-2,3,5,10b-tetraaza-benzo[e]azulene

Base Information

Chemical Name:8-Chloro-6-phenyl-1-pyrrolidin-1-ylmethyl-4H-2,3,5,10b-tetraaza-benzo[e]azulene
CAS No.:38539-19-4
Molecular Formula:C₂₁H₂₀ClN₅
Molecular Weight:377.876
Hs Code.:

Synonyms:8-Chloro-6-phenyl-1-pyrrolidin-1-ylmethyl-4H-2,3,5,10b-tetraaza-benzo[e]azulene

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Chemical Property of 8-Chloro-6-phenyl-1-pyrrolidin-1-ylmethyl-4H-2,3,5,10b-tetraaza-benzo[e]azulene

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Technology Process of 8-Chloro-6-phenyl-1-pyrrolidin-1-ylmethyl-4H-2,3,5,10b-tetraaza-benzo[e]azulene

There total 3 articles about 8-Chloro-6-phenyl-1-pyrrolidin-1-ylmethyl-4H-2,3,5,10b-tetraaza-benzo[e]azulene 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: 72.5%

: 123-75-1
pyrrolidine

: 39479-72-6
8-chloro-1-(chloromethyl)-6-phenyl-4H-s-triazolo<4,3-a><1,4>benzodiazepine

: 38539-19-4
8-Chloro-6-phenyl-1-pyrrolidin-1-ylmethyl-4H-2,3,5,10b-tetraaza-benzo[e]azulene

Guidance literature:: With potassium iodide; In N,N-dimethyl-formamide; at 25 ℃; for 18h;
DOI:10.1021/jm00178a009

Reference yield:

: Chloro-acetic acid N'-(7-chloro-5-phenyl-3H-benzo[e][1,4]diazepin-2-yl)-hydrazide

: 38539-19-4
8-Chloro-6-phenyl-1-pyrrolidin-1-ylmethyl-4H-2,3,5,10b-tetraaza-benzo[e]azulene

Guidance literature:: Multi-step reaction with 2 steps

1: acetic acid / 0.33 h / Heating

2: 72.5 percent / KI / dimethylformamide / 18 h / 25 °C

With potassium iodide; In acetic acid; N,N-dimethyl-formamide;
DOI:10.1021/jm00178a009

Reference yield:

: 18091-89-9,112393-62-1
7-chloro-2-hydrazino-5-phenyl-3H-1,4-benzodiazepine

: 38539-19-4
8-Chloro-6-phenyl-1-pyrrolidin-1-ylmethyl-4H-2,3,5,10b-tetraaza-benzo[e]azulene

Guidance literature:: Multi-step reaction with 3 steps

1: tetrahydrofuran / 1.58 h / 0 - 20 °C

2: acetic acid / 0.33 h / Heating

3: 72.5 percent / KI / dimethylformamide / 18 h / 25 °C

With potassium iodide; In tetrahydrofuran; acetic acid; N,N-dimethyl-formamide;
DOI:10.1021/jm00178a009