3-(aminomethyl)-6-methoxy-2-(2-methylpropyl)-4-phenylisoquinolin-1(2H)-one

Base Information

Chemical Name:3-(aminomethyl)-6-methoxy-2-(2-methylpropyl)-4-phenylisoquinolin-1(2H)-one
CAS No.:447416-03-7
Molecular Formula:C₂₁H₂₄N₂O₂
Molecular Weight:336.434
Hs Code.:

Synonyms:3-(aminomethyl)-6-methoxy-2-(2-methylpropyl)-4-phenylisoquinolin-1(2H)-one

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Chemical Property of 3-(aminomethyl)-6-methoxy-2-(2-methylpropyl)-4-phenylisoquinolin-1(2H)-one

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Technology Process of 3-(aminomethyl)-6-methoxy-2-(2-methylpropyl)-4-phenylisoquinolin-1(2H)-one

There total 12 articles about 3-(aminomethyl)-6-methoxy-2-(2-methylpropyl)-4-phenylisoquinolin-1(2H)-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:

: C₂₂H₂₅NO₅S

: 447416-03-7
3-(aminomethyl)-6-methoxy-2-(2-methylpropyl)-4-phenylisoquinolin-1(2H)-one

Guidance literature:: With ammonia; In tetrahydrofuran; methanol; at 150 ℃; for 6h; Sealed tube;
DOI:10.1016/j.bmc.2011.06.059

Reference yield:

: C₂₁H₁₉FO₇

: 447416-03-7
3-(aminomethyl)-6-methoxy-2-(2-methylpropyl)-4-phenylisoquinolin-1(2H)-one

Guidance literature:: Multi-step reaction with 8 steps

1: hydrogenchloride; water; acetic acid / 3 h / 110 °C

2: methanol / 15 h / 20 °C

3: hydrogenchloride / ethyl acetate / 3 h / 20 °C

4: methanol / 15 h / Reflux

5: oxalyl dichloride; N,N-dimethyl-formamide / tetrahydrofuran / 2 h / 20 °C

6: sodium tetrahydroborate / tetrahydrofuran; 1,2-dimethoxyethane / 2 h / 0 °C

7: triethylamine / dichloromethane / 0.5 h / 20 °C

8: ammonia / tetrahydrofuran; methanol / 6 h / 150 °C / Sealed tube

With hydrogenchloride; sodium tetrahydroborate; oxalyl dichloride; ammonia; water; acetic acid; triethylamine; N,N-dimethyl-formamide; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; dichloromethane; ethyl acetate;
DOI:10.1016/j.bmc.2011.06.059

Reference yield:

: 583837-88-1
6-fluoro-1-oxo-4-phenyl-1H-isochromene-3-carboxylic acid

: 447416-03-7
3-(aminomethyl)-6-methoxy-2-(2-methylpropyl)-4-phenylisoquinolin-1(2H)-one

Guidance literature:: Multi-step reaction with 7 steps

1: methanol / 15 h / 20 °C

2: hydrogenchloride / ethyl acetate / 3 h / 20 °C

3: methanol / 15 h / Reflux

4: oxalyl dichloride; N,N-dimethyl-formamide / tetrahydrofuran / 2 h / 20 °C

5: sodium tetrahydroborate / tetrahydrofuran; 1,2-dimethoxyethane / 2 h / 0 °C

6: triethylamine / dichloromethane / 0.5 h / 20 °C

7: ammonia / tetrahydrofuran; methanol / 6 h / 150 °C / Sealed tube

With hydrogenchloride; sodium tetrahydroborate; oxalyl dichloride; ammonia; triethylamine; N,N-dimethyl-formamide; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; dichloromethane; ethyl acetate;
DOI:10.1016/j.bmc.2011.06.059