6-methoxy-3-{4-[2-(1-piperidinyl)ethoxy]phenoxy}-2-(4-((2-chloroethyl)amino)phenyl)benzo[b]thiophene

Base Information

Chemical Name:6-methoxy-3-{4-[2-(1-piperidinyl)ethoxy]phenoxy}-2-(4-((2-chloroethyl)amino)phenyl)benzo[b]thiophene
CAS No.:943439-60-9
Molecular Formula:C₃₀H₃₃ClN₂O₃S
Molecular Weight:537.123
Hs Code.:

Synonyms:6-methoxy-3-{4-[2-(1-piperidinyl)ethoxy]phenoxy}-2-(4-((2-chloroethyl)amino)phenyl)benzo[b]thiophene

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Chemical Property of 6-methoxy-3-{4-[2-(1-piperidinyl)ethoxy]phenoxy}-2-(4-((2-chloroethyl)amino)phenyl)benzo[b]thiophene

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Technology Process of 6-methoxy-3-{4-[2-(1-piperidinyl)ethoxy]phenoxy}-2-(4-((2-chloroethyl)amino)phenyl)benzo[b]thiophene

There total 8 articles about 6-methoxy-3-{4-[2-(1-piperidinyl)ethoxy]phenoxy}-2-(4-((2-chloroethyl)amino)phenyl)benzo[b]thiophene 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: 37.3%

: 107-20-0
2-chloroethanal

: 943439-57-4
6-methoxy-3-{4-[2-(1-piperidinyl)ethoxy]phenoxy}-2-(4-aminophenyl)benzo[b]thiophene

: 943439-60-9
6-methoxy-3-{4-[2-(1-piperidinyl)ethoxy]phenoxy}-2-(4-((2-chloroethyl)amino)phenyl)benzo[b]thiophene

Guidance literature:: With hydrogenchloride; sodium cyanoborohydride; In methanol; water; at 20 ℃; for 72h;
DOI:10.1021/jm070079j

Reference yield:

: 943439-53-0
6-methoxy-2-(4-bromophenyl)-3-bromobenzo[b]thiophene

: 943439-60-9
6-methoxy-3-{4-[2-(1-piperidinyl)ethoxy]phenoxy}-2-(4-((2-chloroethyl)amino)phenyl)benzo[b]thiophene

Guidance literature:: Multi-step reaction with 5 steps

1.1: 65 percent / TFA; aq. H₂O₂ / CH₂Cl₂ / 2 h / 20 °C

2.1: NaH / dimethylformamide / 0.33 h

2.2: 94 percent / dimethylformamide / 1 h / 20 °C

3.1: HCl / CH₂Cl₂; diethyl ether / 1 h

3.2: 85 percent / TMSCl; Ph₃P / tetrahydrofuran / 8 h / Heating

4.1: 74 percent / NaN₃; NaOH / CuI; L-proline / dimethylsulfoxide; ethanol / 10 h / 110 °C

5.1: 37.3 percent / NaBH₃CN; HCl / methanol; H₂O / 72 h / 20 °C

With hydrogenchloride; sodium hydroxide; sodium azide; dihydrogen peroxide; sodium hydride; sodium cyanoborohydride; trifluoroacetic acid; copper(l) iodide; L-proline; In methanol; diethyl ether; ethanol; dichloromethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide;
DOI:10.1021/jm070079j

Reference yield:

: 943439-52-9
2-(4-bromo-phenyl)-6-methoxy-benzo[b]thiophene

: 943439-60-9
6-methoxy-3-{4-[2-(1-piperidinyl)ethoxy]phenoxy}-2-(4-((2-chloroethyl)amino)phenyl)benzo[b]thiophene

Guidance literature:: Multi-step reaction with 6 steps

1.1: 95 percent / N-bromoacetamide / CH₂Cl₂ / 2 h / 20 °C

2.1: 65 percent / TFA; aq. H₂O₂ / CH₂Cl₂ / 2 h / 20 °C

3.1: NaH / dimethylformamide / 0.33 h

3.2: 94 percent / dimethylformamide / 1 h / 20 °C

4.1: HCl / CH₂Cl₂; diethyl ether / 1 h

4.2: 85 percent / TMSCl; Ph₃P / tetrahydrofuran / 8 h / Heating

5.1: 74 percent / NaN₃; NaOH / CuI; L-proline / dimethylsulfoxide; ethanol / 10 h / 110 °C

6.1: 37.3 percent / NaBH₃CN; HCl / methanol; H₂O / 72 h / 20 °C

With hydrogenchloride; sodium hydroxide; sodium azide; dihydrogen peroxide; sodium hydride; sodium cyanoborohydride; trifluoroacetic acid; N-bromoacetamide; copper(l) iodide; L-proline; In methanol; diethyl ether; ethanol; dichloromethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide;
DOI:10.1021/jm070079j