6-[4-(1-{[(3R)-1-(cyclopropylcarbonyl)-3-pyrrolidinyl]methyl}-1H-tetrazol-5-yl)phenyl]-1H-indole

Base Information

Chemical Name:6-[4-(1-{[(3R)-1-(cyclopropylcarbonyl)-3-pyrrolidinyl]methyl}-1H-tetrazol-5-yl)phenyl]-1H-indole
CAS No.:1366766-52-0
Molecular Formula:C₂₄H₂₄N₆O
Molecular Weight:412.494
Hs Code.:

Synonyms:6-[4-(1-{[(3R)-1-(cyclopropylcarbonyl)-3-pyrrolidinyl]methyl}-1H-tetrazol-5-yl)phenyl]-1H-indole

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Chemical Property of 6-[4-(1-{[(3R)-1-(cyclopropylcarbonyl)-3-pyrrolidinyl]methyl}-1H-tetrazol-5-yl)phenyl]-1H-indole

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Technology Process of 6-[4-(1-{[(3R)-1-(cyclopropylcarbonyl)-3-pyrrolidinyl]methyl}-1H-tetrazol-5-yl)phenyl]-1H-indole

There total 9 articles about 6-[4-(1-{[(3R)-1-(cyclopropylcarbonyl)-3-pyrrolidinyl]methyl}-1H-tetrazol-5-yl)phenyl]-1H-indole 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: 92.0%

: 1366767-74-9
5-(4-bromophenyl)-1-{[(3R)-1-(cyclopropylcarbonyl)-3-pyrrolidinyl]methyl}-1H-tetrazole

: 147621-18-9
6-indolylboronic acid

: 1366766-52-0
6-[4-(1-{[(3R)-1-(cyclopropylcarbonyl)-3-pyrrolidinyl]methyl}-1H-tetrazol-5-yl)phenyl]-1H-indole

Guidance literature:: With sodium carbonate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In 1,2-dimethoxyethane; water; at 100 ℃; for 0.75h; Inert atmosphere; microwave irradiation;

Reference yield:

: 586-76-5
4-Bromobenzoic acid

: 1366766-52-0
6-[4-(1-{[(3R)-1-(cyclopropylcarbonyl)-3-pyrrolidinyl]methyl}-1H-tetrazol-5-yl)phenyl]-1H-indole

Guidance literature:: Multi-step reaction with 5 steps

1.1: N,N-dimethyl-formamide; oxalyl dichloride / dichloromethane / 2 h / 25 °C

1.2: 20 °C / Cooling with ice

2.1: trimethylsilylazide; triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 25 °C

3.1: hydrogenchloride / 1,4-dioxane / 0.5 h / 25 °C

4.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 1 h / 25 °C

5.1: sodium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,2-dimethoxyethane; water / 0.75 h / 100 °C / Inert atmosphere; microwave irradiation

With hydrogenchloride; oxalyl dichloride; trimethylsilylazide; di-isopropyl azodicarboxylate; sodium carbonate; N-ethyl-N,N-diisopropylamine; N,N-dimethyl-formamide; triphenylphosphine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; 1,2-dimethoxyethane; dichloromethane; water;

Reference yield:

: 199175-10-5
1,1-dimethylethyl (3S)-3-(aminomethyl)-1-pyrrolidinecarboxylate

: 1366766-52-0
6-[4-(1-{[(3R)-1-(cyclopropylcarbonyl)-3-pyrrolidinyl]methyl}-1H-tetrazol-5-yl)phenyl]-1H-indole

Guidance literature:: Multi-step reaction with 5 steps

1.1: N,N-dimethyl-formamide; oxalyl dichloride / dichloromethane / 2 h / 25 °C

1.2: 20 °C / Cooling with ice

2.1: trimethylsilylazide; triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 25 °C

3.1: hydrogenchloride / 1,4-dioxane / 0.5 h / 25 °C

4.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 1 h / 25 °C

5.1: sodium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,2-dimethoxyethane; water / 0.75 h / 100 °C / Inert atmosphere; microwave irradiation

With hydrogenchloride; oxalyl dichloride; trimethylsilylazide; di-isopropyl azodicarboxylate; sodium carbonate; N-ethyl-N,N-diisopropylamine; N,N-dimethyl-formamide; triphenylphosphine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; 1,2-dimethoxyethane; dichloromethane; water;