7-{3-[2-amino-5-(methoxymethoxy)phenyl]-1-hydroxypropyl}naphthalene-2-carbonitrile

Base Information

Chemical Name:7-{3-[2-amino-5-(methoxymethoxy)phenyl]-1-hydroxypropyl}naphthalene-2-carbonitrile
CAS No.:319451-66-6
Molecular Formula:C₂₂H₂₂N₂O₃
Molecular Weight:362.428
Hs Code.:

Synonyms:7-{3-[2-amino-5-(methoxymethoxy)phenyl]-1-hydroxypropyl}naphthalene-2-carbonitrile

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Chemical Property of 7-{3-[2-amino-5-(methoxymethoxy)phenyl]-1-hydroxypropyl}naphthalene-2-carbonitrile

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Technology Process of 7-{3-[2-amino-5-(methoxymethoxy)phenyl]-1-hydroxypropyl}naphthalene-2-carbonitrile

There total 9 articles about 7-{3-[2-amino-5-(methoxymethoxy)phenyl]-1-hydroxypropyl}naphthalene-2-carbonitrile 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: 84.0%

: 7-{1-hydroxy-3-[5-(methoxymethoxy)-2-nitrophenyl]-2-propene-1-yl}naphthalene-2-carbonitrile

: 319451-66-6
7-{3-[2-amino-5-(methoxymethoxy)phenyl]-1-hydroxypropyl}naphthalene-2-carbonitrile

Guidance literature:: With hydrogen; palladium on activated charcoal; In tetrahydrofuran; ethanol; at 20 ℃; for 5h;
DOI:10.1248/cpb.54.163

Reference yield:

: 319452-67-0
7-acetylnaphthalene-2-carbonitrile

: 319451-66-6
7-{3-[2-amino-5-(methoxymethoxy)phenyl]-1-hydroxypropyl}naphthalene-2-carbonitrile

Guidance literature:: Multi-step reaction with 5 steps

1.1: lithium diisopropylamide / tetrahydrofuran; heptane; ethylbenzene / 0.25 h / -65 °C

1.2: 59 percent / tetrahydrofuran; heptane; ethylbenzene / 3 h / -65 °C

2.1: p-TsOH*H₂O / 1,2-dichloro-ethane / 2 h / Heating

3.1: 5.32 g / Et₃N / N,N-dimethyl-acetamide / 4 h / 0 °C

4.1: 64 percent / NaBH₄ / CH₂Cl₂; ethanol / 3 h / 20 °C

5.1: 84 percent / H₂ / Pd/C / ethanol; tetrahydrofuran / 5 h / 20 °C

With sodium tetrahydroborate; hydrogen; toluene-4-sulfonic acid; triethylamine; lithium diisopropyl amide; palladium on activated charcoal; In tetrahydrofuran; ethanol; n-heptane; dichloromethane; N,N-dimethyl acetamide; ethylbenzene; 1,2-dichloro-ethane;
DOI:10.1248/cpb.54.163

Reference yield:

: 170991-12-5
2-formyl-4-(methoxymethoxy)-1-nitrobenzene

: 319451-66-6
7-{3-[2-amino-5-(methoxymethoxy)phenyl]-1-hydroxypropyl}naphthalene-2-carbonitrile

Guidance literature:: Multi-step reaction with 5 steps

1.1: lithium diisopropylamide / tetrahydrofuran; heptane; ethylbenzene / 0.25 h / -65 °C

1.2: 59 percent / tetrahydrofuran; heptane; ethylbenzene / 3 h / -65 °C

2.1: p-TsOH*H₂O / 1,2-dichloro-ethane / 2 h / Heating

3.1: 5.32 g / Et₃N / N,N-dimethyl-acetamide / 4 h / 0 °C

4.1: 64 percent / NaBH₄ / CH₂Cl₂; ethanol / 3 h / 20 °C

5.1: 84 percent / H₂ / Pd/C / ethanol; tetrahydrofuran / 5 h / 20 °C

With sodium tetrahydroborate; hydrogen; toluene-4-sulfonic acid; triethylamine; lithium diisopropyl amide; palladium on activated charcoal; In tetrahydrofuran; ethanol; n-heptane; dichloromethane; N,N-dimethyl acetamide; ethylbenzene; 1,2-dichloro-ethane;
DOI:10.1248/cpb.54.163