(6-benzenesulfonyl-1,2,3,4-tetrahydro-naphthalen-1-ylmethyl)-(4,5-dihydro-1H-imidazol-2-yl)-amine

Base Information

Chemical Name:(6-benzenesulfonyl-1,2,3,4-tetrahydro-naphthalen-1-ylmethyl)-(4,5-dihydro-1H-imidazol-2-yl)-amine
CAS No.:880544-27-4
Molecular Formula:C₂₀H₂₃N₃O₂S
Molecular Weight:369.488
Hs Code.:

Synonyms:(6-benzenesulfonyl-1,2,3,4-tetrahydro-naphthalen-1-ylmethyl)-(4,5-dihydro-1H-imidazol-2-yl)-amine

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Chemical Property of (6-benzenesulfonyl-1,2,3,4-tetrahydro-naphthalen-1-ylmethyl)-(4,5-dihydro-1H-imidazol-2-yl)-amine

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Technology Process of (6-benzenesulfonyl-1,2,3,4-tetrahydro-naphthalen-1-ylmethyl)-(4,5-dihydro-1H-imidazol-2-yl)-amine

There total 11 articles about (6-benzenesulfonyl-1,2,3,4-tetrahydro-naphthalen-1-ylmethyl)-(4,5-dihydro-1H-imidazol-2-yl)-amine 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: 47.0%

: 880544-30-9
C-(6-benzenesulfonyl-1,2,3,4-tetrahydro-naphthalen-1-yl)-methylamine

: 5464-11-9
2-methylthio-2-imidazoline hydroiodide

: 880544-27-4
(6-benzenesulfonyl-1,2,3,4-tetrahydro-naphthalen-1-ylmethyl)-(4,5-dihydro-1H-imidazol-2-yl)-amine

Guidance literature:: C-(6-benzenesulfonyl-1,2,3,4-tetrahydro-naphthalen-1-yl)-methylamine; 2-methylthio-2-imidazoline hydroiodide; In dichloromethane; at 150 ℃; for 0.5h; Heating / reflux;

With sodium hydroxide; In water;

Reference yield:

: 149915-80-0
6-phenylsulfanyl-3,4-dihydro-2H-naphthalen-1-one

: 880544-27-4
(6-benzenesulfonyl-1,2,3,4-tetrahydro-naphthalen-1-ylmethyl)-(4,5-dihydro-1H-imidazol-2-yl)-amine

Guidance literature:: Multi-step reaction with 5 steps

1.1: Oxone / methanol; water; acetonitrile / 15 h / 20 °C

2.1: zinc(II) iodide / 15 h

2.2: 3 h / Heating / reflux

3.1: hydrogen; acetic acid / palladium 10% on activated carbon / ethanol / 15 h / 2844.39 Torr

4.1: borane-THF / tetrahydrofuran / 15 h / 0 - 20 °C

5.1: dichloromethane / 0.5 h / 150 °C

With Oxone; borane-THF; hydrogen; acetic acid; zinc(II) iodide; palladium 10% on activated carbon; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; acetonitrile;

Reference yield:

: 895132-99-7
6-Benzenesulfonyl-3,4-dihydro-2H-naphthalen-1-one

: 880544-27-4
(6-benzenesulfonyl-1,2,3,4-tetrahydro-naphthalen-1-ylmethyl)-(4,5-dihydro-1H-imidazol-2-yl)-amine

Guidance literature:: Multi-step reaction with 4 steps

1.1: zinc(II) iodide / 15 h

1.2: 3 h / Heating / reflux

2.1: hydrogen; acetic acid / palladium 10% on activated carbon / ethanol / 15 h / 2844.39 Torr

3.1: borane-THF / tetrahydrofuran / 15 h / 0 - 20 °C

4.1: dichloromethane / 0.5 h / 150 °C

With borane-THF; hydrogen; acetic acid; zinc(II) iodide; palladium 10% on activated carbon; In tetrahydrofuran; ethanol; dichloromethane;