1-{5-chloro-2-[(4-chloro-2-fluorobenzyl)oxy]benzyl}-4-(1H-tetrazol-5-yl)-2,3-dihydro-1H-pyrrolo[2,3-b]pyridine

Base Information

Chemical Name:1-{5-chloro-2-[(4-chloro-2-fluorobenzyl)oxy]benzyl}-4-(1H-tetrazol-5-yl)-2,3-dihydro-1H-pyrrolo[2,3-b]pyridine
CAS No.:1428128-63-5
Molecular Formula:C₂₂H₁₇Cl₂FN₆O
Molecular Weight:471.321
Hs Code.:

Synonyms:1-{5-chloro-2-[(4-chloro-2-fluorobenzyl)oxy]benzyl}-4-(1H-tetrazol-5-yl)-2,3-dihydro-1H-pyrrolo[2,3-b]pyridine

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Chemical Property of 1-{5-chloro-2-[(4-chloro-2-fluorobenzyl)oxy]benzyl}-4-(1H-tetrazol-5-yl)-2,3-dihydro-1H-pyrrolo[2,3-b]pyridine

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Technology Process of 1-{5-chloro-2-[(4-chloro-2-fluorobenzyl)oxy]benzyl}-4-(1H-tetrazol-5-yl)-2,3-dihydro-1H-pyrrolo[2,3-b]pyridine

There total 7 articles about 1-{5-chloro-2-[(4-chloro-2-fluorobenzyl)oxy]benzyl}-4-(1H-tetrazol-5-yl)-2,3-dihydro-1H-pyrrolo[2,3-b]pyridine 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: 37.0%

: 1428130-75-9
1-{5-chloro-2-[(4-chloro-2-fluorobenzyl)oxy]benzyl}-2,3-dihydro-1H-pyrrolo[2,3-b]pyridine-4-carbonitrile

: 1428128-63-5
1-{5-chloro-2-[(4-chloro-2-fluorobenzyl)oxy]benzyl}-4-(1H-tetrazol-5-yl)-2,3-dihydro-1H-pyrrolo[2,3-b]pyridine

Guidance literature:: With trimethylsilylazide; di(n-butyl)tin oxide; In toluene; at 120 ℃; for 22h; Sealed tube;

Reference yield:

: 1428129-54-7
3-{5-chloro-2-[(4-chloro-2-fluorobenzyl)oxy]benzyl}-1,2,3-oxathiazolidine 2-oxide

: 1428128-63-5
1-{5-chloro-2-[(4-chloro-2-fluorobenzyl)oxy]benzyl}-4-(1H-tetrazol-5-yl)-2,3-dihydro-1H-pyrrolo[2,3-b]pyridine

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium periodate; ruthenium(III) trichloride hydrate / water; acetonitrile / 7 h / 20 °C

2.1: lithium diisopropyl amide / tetrahydrofuran / 1.5 h / -78 °C

2.2: 20 °C

3.1: potassium carbonate / N,N-dimethyl-formamide / 4 h / 100 °C

4.1: tetrakis(triphenylphosphine) palladium⁽⁰⁾ / N,N-dimethyl-formamide / 16 h / 90 °C / Inert atmosphere

5.1: trimethylsilylazide; di(n-butyl)tin oxide / toluene / 22 h / 120 °C / Sealed tube

With sodium periodate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; ruthenium(III) trichloride hydrate; trimethylsilylazide; di(n-butyl)tin oxide; potassium carbonate; lithium diisopropyl amide; In tetrahydrofuran; water; N,N-dimethyl-formamide; toluene; acetonitrile;

Reference yield:

: 1428129-52-5
3-{5-chloro-2-[(4-chloro-2-fluorobenzyl)oxy]benzyl}-1,2,3-oxathiazolidine 2,2-dioxide

: 1428128-63-5
1-{5-chloro-2-[(4-chloro-2-fluorobenzyl)oxy]benzyl}-4-(1H-tetrazol-5-yl)-2,3-dihydro-1H-pyrrolo[2,3-b]pyridine

Guidance literature:: Multi-step reaction with 4 steps

1.1: lithium diisopropyl amide / tetrahydrofuran / 1.5 h / -78 °C

1.2: 20 °C

2.1: potassium carbonate / N,N-dimethyl-formamide / 4 h / 100 °C

3.1: tetrakis(triphenylphosphine) palladium⁽⁰⁾ / N,N-dimethyl-formamide / 16 h / 90 °C / Inert atmosphere

4.1: trimethylsilylazide; di(n-butyl)tin oxide / toluene / 22 h / 120 °C / Sealed tube

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; trimethylsilylazide; di(n-butyl)tin oxide; potassium carbonate; lithium diisopropyl amide; In tetrahydrofuran; N,N-dimethyl-formamide; toluene;