methyl 5-methanesulfonylamino-2-(2-methoxy-6-methoxymethoxyphenyl)-benzoate

Base Information

Chemical Name:methyl 5-methanesulfonylamino-2-(2-methoxy-6-methoxymethoxyphenyl)-benzoate
CAS No.:373623-09-7
Molecular Formula:C₁₈H₂₁NO₇S
Molecular Weight:395.433
Hs Code.:

Synonyms:methyl 5-methanesulfonylamino-2-(2-methoxy-6-methoxymethoxyphenyl)-benzoate

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Chemical Property of methyl 5-methanesulfonylamino-2-(2-methoxy-6-methoxymethoxyphenyl)-benzoate

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Technology Process of methyl 5-methanesulfonylamino-2-(2-methoxy-6-methoxymethoxyphenyl)-benzoate

There total 1 articles about methyl 5-methanesulfonylamino-2-(2-methoxy-6-methoxymethoxyphenyl)-benzoate 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:

: 57234-28-3
1-methoxy-3-(methoxymethoxy)benzene

: 373623-09-7
methyl 5-methanesulfonylamino-2-(2-methoxy-6-methoxymethoxyphenyl)-benzoate

Guidance literature:: Multi-step reaction with 3 steps

1.1: n-BuLi / hexane; tetrahydrofuran / 1 h / -30 - 20 °C

1.2: ZnCl₂ / hexane; tetrahydrofuran / 2 h / 0 - 20 °C

1.3: Pd(PPh₃)2Cl₂ / 65 °C

2.1: Fe; NH₄Cl / aq. ethanol / 95 °C

3.1: pyridine / 0 - 20 °C

With pyridine; n-butyllithium; iron; ammonium chloride; In tetrahydrofuran; ethanol; hexane;
DOI:10.1016/j.bmcl.2004.02.048

Reference yield:

: 373623-09-7
methyl 5-methanesulfonylamino-2-(2-methoxy-6-methoxymethoxyphenyl)-benzoate

: N-(6-cyclohexyl-1-methoxy-6H-benzo[c]chromen-8-yl)-methanesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1: DIBAL / heptane; CH₂Cl₂ / -78 - 0 °C

2: TPAP; NMO / acetonitrile / 20 °C

3: 99 percent / p-TsOH / methanol / 3 h / 20 °C

4: BF₃*Et₂O / CH₂Cl₂ / -10 °C

With N-methyl-2-indolinone; tetrapropylammonium perruthennate; boron trifluoride diethyl etherate; diisobutylaluminium hydride; toluene-4-sulfonic acid; In methanol; n-heptane; dichloromethane; acetonitrile;
DOI:10.1016/j.bmcl.2004.02.048

Reference yield:

: 373623-09-7
methyl 5-methanesulfonylamino-2-(2-methoxy-6-methoxymethoxyphenyl)-benzoate

: 373622-16-3
N-{1-methoxy-6-[3-(methylamino)phenyl]-6H-benzo[c]chromen-8-yl}methanesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1: DIBAL / heptane; CH₂Cl₂ / -78 - 0 °C

2: TPAP; NMO / acetonitrile / 20 °C

3: 99 percent / p-TsOH / methanol / 3 h / 20 °C

4: BF₃*Et₂O / CH₂Cl₂ / -10 °C

With N-methyl-2-indolinone; tetrapropylammonium perruthennate; boron trifluoride diethyl etherate; diisobutylaluminium hydride; toluene-4-sulfonic acid; In methanol; n-heptane; dichloromethane; acetonitrile;
DOI:10.1016/j.bmcl.2004.02.048