methyl 6-[6-({[3-(2,6-dichlorophenyl)-5-(1-methylethyl)-4-isoxazolyl]methyl}oxy)-3-pyridinyl]-1H-indole-3-carboxylate

Base Information

Chemical Name:methyl 6-[6-({[3-(2,6-dichlorophenyl)-5-(1-methylethyl)-4-isoxazolyl]methyl}oxy)-3-pyridinyl]-1H-indole-3-carboxylate
CAS No.:1093631-89-0
Molecular Formula:C₂₈H₂₃Cl₂N₃O₄
Molecular Weight:536.414
Hs Code.:

Synonyms:methyl 6-[6-({[3-(2,6-dichlorophenyl)-5-(1-methylethyl)-4-isoxazolyl]methyl}oxy)-3-pyridinyl]-1H-indole-3-carboxylate

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Chemical Property of methyl 6-[6-({[3-(2,6-dichlorophenyl)-5-(1-methylethyl)-4-isoxazolyl]methyl}oxy)-3-pyridinyl]-1H-indole-3-carboxylate

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Technology Process of methyl 6-[6-({[3-(2,6-dichlorophenyl)-5-(1-methylethyl)-4-isoxazolyl]methyl}oxy)-3-pyridinyl]-1H-indole-3-carboxylate

There total 5 articles about methyl 6-[6-({[3-(2,6-dichlorophenyl)-5-(1-methylethyl)-4-isoxazolyl]methyl}oxy)-3-pyridinyl]-1H-indole-3-carboxylate 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:

: 700835-81-0
4-(chloromethyl)-3-(2,6-dichlorophenyl)-5-(propan-2-yl)-1,2-oxazole

: 1093631-88-9
methyl 6-(6-fluoro-3-pyridinyl)-1H-indole-3-carboxylate

: 1093631-89-0
methyl 6-[6-({[3-(2,6-dichlorophenyl)-5-(1-methylethyl)-4-isoxazolyl]methyl}oxy)-3-pyridinyl]-1H-indole-3-carboxylate

Guidance literature:: With potassium tert-butylate; In tert-butyl alcohol; at 20 - 80 ℃; Inert atmosphere;

Reference yield:

: 52415-29-9
6-bromo-1H-indole

: 1093631-89-0
methyl 6-[6-({[3-(2,6-dichlorophenyl)-5-(1-methylethyl)-4-isoxazolyl]methyl}oxy)-3-pyridinyl]-1H-indole-3-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: trichlorophosphate / 0.5 h / 0 - 8 °C / Inert atmosphere

1.2: 2 h / 0 - 20 °C

2.1: sodium cyanide / 0.08 h / 20 °C

2.2: 20 °C / Inert atmosphere

3.1: sodium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,2-dimethoxyethane / 15 h / Inert atmosphere; Reflux

4.1: potassium tert-butylate / tert-butyl alcohol / 20 - 80 °C / Inert atmosphere

With sodium cyanide; potassium tert-butylate; sodium carbonate; trichlorophosphate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In 1,2-dimethoxyethane; tert-butyl alcohol; 3.1: Suzuki Coupling;

Reference yield:

: 17826-04-9
6-bromo-1H-indole-3-carbaldehyde

: 1093631-89-0
methyl 6-[6-({[3-(2,6-dichlorophenyl)-5-(1-methylethyl)-4-isoxazolyl]methyl}oxy)-3-pyridinyl]-1H-indole-3-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium cyanide / 0.08 h / 20 °C

1.2: 20 °C / Inert atmosphere

2.1: sodium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,2-dimethoxyethane / 15 h / Inert atmosphere; Reflux

3.1: potassium tert-butylate / tert-butyl alcohol / 20 - 80 °C / Inert atmosphere

With sodium cyanide; potassium tert-butylate; sodium carbonate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In 1,2-dimethoxyethane; tert-butyl alcohol; 2.1: Suzuki Coupling;