6-Pyrrolidin-1-yl-3-(2,4,5-trimethoxy-phenyl)-[1,2,4]triazolo[3,4-a]phthalazine

Base Information

Chemical Name:6-Pyrrolidin-1-yl-3-(2,4,5-trimethoxy-phenyl)-[1,2,4]triazolo[3,4-a]phthalazine
CAS No.:113628-66-3
Molecular Formula:C₂₂H₂₃N₅O₃
Molecular Weight:405.456
Hs Code.:

Synonyms:6-Pyrrolidin-1-yl-3-(2,4,5-trimethoxy-phenyl)-[1,2,4]triazolo[3,4-a]phthalazine

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Chemical Property of 6-Pyrrolidin-1-yl-3-(2,4,5-trimethoxy-phenyl)-[1,2,4]triazolo[3,4-a]phthalazine

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Technology Process of 6-Pyrrolidin-1-yl-3-(2,4,5-trimethoxy-phenyl)-[1,2,4]triazolo[3,4-a]phthalazine

There total 4 articles about 6-Pyrrolidin-1-yl-3-(2,4,5-trimethoxy-phenyl)-[1,2,4]triazolo[3,4-a]phthalazine 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: 79.0%

: 123-75-1
pyrrolidine

: 113628-56-1
6-Chloro-3-(2,4,5-trimethoxy-phenyl)-[1,2,4]triazolo[3,4-a]phthalazine

: 113628-66-3,87540-15-6
6-Pyrrolidin-1-yl-3-(2,4,5-trimethoxy-phenyl)-[1,2,4]triazolo[3,4-a]phthalazine

Guidance literature:: at 140 ℃; for 30h;
DOI:10.1021/jm00401a010

Reference yield:

: 51935-42-3,59275-72-8
1-chloro-4-hydrazinophthalazine

: 113628-66-3,87540-15-6
6-Pyrrolidin-1-yl-3-(2,4,5-trimethoxy-phenyl)-[1,2,4]triazolo[3,4-a]phthalazine

Guidance literature:: Multi-step reaction with 3 steps

1: 91 percent / 0.1N HCl / 0.17 h / 60 °C

2: 73 percent / Br₂, sodium acetate / acetic acid / 1 h / Ambient temperature

3: 79 percent / 30 h / 140 °C

With hydrogenchloride; bromine; sodium acetate; In acetic acid;
DOI:10.1021/jm00401a010

Reference yield:

: 4460-86-0,14374-62-0
asaraldehyde

: 113628-66-3,87540-15-6
6-Pyrrolidin-1-yl-3-(2,4,5-trimethoxy-phenyl)-[1,2,4]triazolo[3,4-a]phthalazine

Guidance literature:: Multi-step reaction with 3 steps

1: 91 percent / 0.1N HCl / 0.17 h / 60 °C

2: 73 percent / Br₂, sodium acetate / acetic acid / 1 h / Ambient temperature

3: 79 percent / 30 h / 140 °C

With hydrogenchloride; bromine; sodium acetate; In acetic acid;
DOI:10.1021/jm00401a010