2-[2-cyclobutyl-1-(4-methanesulfonyl-phenyl)-ethyl]-5-fluoro-1H-pyrrolo[2,3-b]pyridine

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Chemical Name:2-[2-cyclobutyl-1-(4-methanesulfonyl-phenyl)-ethyl]-5-fluoro-1H-pyrrolo[2,3-b]pyridine
CAS No.:1312016-79-7
Molecular Formula:C₂₀H₂₁FN₂O₂S
Molecular Weight:372.463
Hs Code.:

Synonyms:2-[2-cyclobutyl-1-(4-methanesulfonyl-phenyl)-ethyl]-5-fluoro-1H-pyrrolo[2,3-b]pyridine

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Chemical Property of 2-[2-cyclobutyl-1-(4-methanesulfonyl-phenyl)-ethyl]-5-fluoro-1H-pyrrolo[2,3-b]pyridine

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Technology Process of 2-[2-cyclobutyl-1-(4-methanesulfonyl-phenyl)-ethyl]-5-fluoro-1H-pyrrolo[2,3-b]pyridine

There total 10 articles about 2-[2-cyclobutyl-1-(4-methanesulfonyl-phenyl)-ethyl]-5-fluoro-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: 17.5%

: 1312016-78-6
2-[(E)-2-cyclobutyl-1-(4-methanesulfonyl-phenyl)-vinyl]-5-fluoro-1H-pyrrolo[2,3-b]pyridine

: 1312016-79-7
2-[2-cyclobutyl-1-(4-methanesulfonyl-phenyl)-ethyl]-5-fluoro-1H-pyrrolo[2,3-b]pyridine

Guidance literature:: With hydrogen; palladium 10% on activated carbon; In methanol; at 50 ℃; for 8h; under 2585.81 Torr;

Reference yield:

: 3446-89-7
4-(Methylthio)benzaldehyde

: 1312016-79-7
2-[2-cyclobutyl-1-(4-methanesulfonyl-phenyl)-ethyl]-5-fluoro-1H-pyrrolo[2,3-b]pyridine

Guidance literature:: Multi-step reaction with 7 steps

1.1: n-butyllithium / hexane; tetrahydrofuran / 0.58 h / -78 °C

1.2: 1 h / -78 °C

2.1: Dess-Martin periodane / dichloromethane / 1 h / 25 °C

3.1: tetrahydrofuran / 1 h / 0 °C

4.1: sodium periodate / water; methanol / 8 h / 20 °C

5.1: potassium permanganate / water; methanol / 2 h / 20 °C

6.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 20 °C

7.1: hydrogen / palladium 10% on activated carbon / methanol / 8 h / 50 °C / 2585.81 Torr

With potassium permanganate; sodium periodate; n-butyllithium; tetrabutyl ammonium fluoride; hydrogen; Dess-Martin periodane; palladium 10% on activated carbon; In tetrahydrofuran; methanol; hexane; dichloromethane; water;

Reference yield:

: 17247-58-4
(Bromomethyl)cyclobutane

: 1312016-79-7
2-[2-cyclobutyl-1-(4-methanesulfonyl-phenyl)-ethyl]-5-fluoro-1H-pyrrolo[2,3-b]pyridine

Guidance literature:: Multi-step reaction with 6 steps

1: iodine; magnesium / tetrahydrofuran / 0.5 h / Reflux

2: tetrahydrofuran / 1 h / 0 °C

3: sodium periodate / water; methanol / 8 h / 20 °C

4: potassium permanganate / water; methanol / 2 h / 20 °C

5: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 20 °C

6: hydrogen / palladium 10% on activated carbon / methanol / 8 h / 50 °C / 2585.81 Torr

With potassium permanganate; sodium periodate; tetrabutyl ammonium fluoride; hydrogen; iodine; magnesium; palladium 10% on activated carbon; In tetrahydrofuran; methanol; water;