1-benzyl-4-chloro-6-trifluoromethyl-1,3-dihydro-imidazo[4,5-c]pyridine-2-one

Base Information

Chemical Name:1-benzyl-4-chloro-6-trifluoromethyl-1,3-dihydro-imidazo[4,5-c]pyridine-2-one
CAS No.:947144-20-9
Molecular Formula:C₁₄H₉ClF₃N₃O
Molecular Weight:327.693
Hs Code.:

Synonyms:1-benzyl-4-chloro-6-trifluoromethyl-1,3-dihydro-imidazo[4,5-c]pyridine-2-one

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Chemical Property of 1-benzyl-4-chloro-6-trifluoromethyl-1,3-dihydro-imidazo[4,5-c]pyridine-2-one

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Technology Process of 1-benzyl-4-chloro-6-trifluoromethyl-1,3-dihydro-imidazo[4,5-c]pyridine-2-one

There total 6 articles about 1-benzyl-4-chloro-6-trifluoromethyl-1,3-dihydro-imidazo[4,5-c]pyridine-2-one 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%

: N₄-Benzyl-2-chloro-6-trifluoromethyl-pyridine-3,4-diamine

: 530-62-1
1,1'-carbonyldiimidazole

: 947144-20-9
1-benzyl-4-chloro-6-trifluoromethyl-1,3-dihydro-imidazo[4,5-c]pyridine-2-one

Guidance literature:: In acetonitrile; at 80 ℃;
DOI:10.1021/op200021a

Reference yield:

: 947144-18-5
benzyl-(2-chloro-3-nitro-6-trifluoromethylpyridin-4-yl)amine

: 947144-20-9
1-benzyl-4-chloro-6-trifluoromethyl-1,3-dihydro-imidazo[4,5-c]pyridine-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: iron; acetic acid / water / 20 °C

2: acetonitrile / 80 °C

With iron; acetic acid; In water; acetonitrile;
DOI:10.1021/op200021a

Reference yield:

: 947144-28-7
4-hydroxy-2-oxo-6-trifluoromethyl-1,2-dihydropyridine-3-carboxylic acid ethyl ester

: 947144-20-9
1-benzyl-4-chloro-6-trifluoromethyl-1,3-dihydro-imidazo[4,5-c]pyridine-2-one

Guidance literature:: Multi-step reaction with 7 steps

1: hydrogenchloride / water / Reflux

2: sulfuric acid; nitric acid / 5.5 h / 20 - 50 °C

3: P,P-dichlorophenylphosphine oxide / dichloromethane / 15 h / 95 °C / Inert atmosphere; Large scale reaction

4: tetrahydrofuran / 22 h / Reflux; Large scale reaction

5: P,P-dichlorophenylphosphine oxide / dichloromethane / 22 h / 95 °C / Inert atmosphere; Large scale reaction

6: iron; acetic acid / water / 20 °C

7: acetonitrile / 80 °C

With P,P-dichlorophenylphosphine oxide; hydrogenchloride; sulfuric acid; nitric acid; iron; acetic acid; In tetrahydrofuran; dichloromethane; water; acetonitrile;
DOI:10.1021/op200021a