N-[(1S,2R)-(2-(1-methyl-1-phenylethyl)cyclohexyloxy)carbonyl]-2-(3,4-dimethoxyphenyl)ethylamine

Base Information

Chemical Name:N-[(1S,2R)-(2-(1-methyl-1-phenylethyl)cyclohexyloxy)carbonyl]-2-(3,4-dimethoxyphenyl)ethylamine
CAS No.:199742-71-7
Molecular Formula:C₂₆H₃₅NO₄
Molecular Weight:425.568
Hs Code.:

Synonyms:N-[(1S,2R)-(2-(1-methyl-1-phenylethyl)cyclohexyloxy)carbonyl]-2-(3,4-dimethoxyphenyl)ethylamine

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Chemical Property of N-[(1S,2R)-(2-(1-methyl-1-phenylethyl)cyclohexyloxy)carbonyl]-2-(3,4-dimethoxyphenyl)ethylamine

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Technology Process of N-[(1S,2R)-(2-(1-methyl-1-phenylethyl)cyclohexyloxy)carbonyl]-2-(3,4-dimethoxyphenyl)ethylamine

There total 1 articles about N-[(1S,2R)-(2-(1-methyl-1-phenylethyl)cyclohexyloxy)carbonyl]-2-(3,4-dimethoxyphenyl)ethylamine 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: 86.0%

: 120-20-7
2-(3,4-dimethoxyphenyl)-ethylamine

: 161693-64-7
(1S,2R)-2-(1-methyl-1-phenylethyl)cyclohexyl chloroformate

: 199742-71-7
N-[(1S,2R)-(2-(1-methyl-1-phenylethyl)cyclohexyloxy)carbonyl]-2-(3,4-dimethoxyphenyl)ethylamine

Guidance literature:: With sodium hydroxide; In dichloromethane; at 25 ℃; for 16h;
DOI:10.1016/S0040-4020(97)01018-1

Reference yield: 75.0%

: 2-bromo-4,5-dimethoxy-1-(2-methoxyethenyl)benzene

: 199742-71-7
N-[(1S,2R)-(2-(1-methyl-1-phenylethyl)cyclohexyloxy)carbonyl]-2-(3,4-dimethoxyphenyl)ethylamine

: 1-[2-bromo-4,5-dimethoxybenzyl]-2-[((1S,2R)-(1-methyl-1-phenylethyl)cyclohexyloxy)carbonyl]-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline

: 199742-72-8
1-[2-bromo-4,5-dimethoxybenzyl]-2-[((1S,2R)-(1-methyl-1-phenylethyl)cyclohexyloxy)carbonyl]-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at -10 - 0 ℃; for 64h;
DOI:10.1016/S0040-4020(97)01018-1

Reference yield:

: 199742-71-7
N-[(1S,2R)-(2-(1-methyl-1-phenylethyl)cyclohexyloxy)carbonyl]-2-(3,4-dimethoxyphenyl)ethylamine

: 109527-45-9
(1S,2R)-(+)-trans-2-(1-methyl-1-phenylethyl)cyclohexanol

Guidance literature:: Multi-step reaction with 2 steps

1: 75 percent / trifluoroacetic acid / CH₂Cl₂ / 64 h / -10 - 0 °C

2: t-BuLi; potassium tert-amylate / tetrahydrofuran; pentane; hexane / 16 h / -78 - 25 °C

With tert.-butyl lithium; potassium 2-methylbutan-2-olate; trifluoroacetic acid; In tetrahydrofuran; hexane; dichloromethane; pentane; 1: Pictet-Spengler reaction / 2: Cyclization;
DOI:10.1016/S0040-4020(97)01018-1