2-fluoro-N-(2-{[(2-hydroxy-2-methylpropyl)amino]methyl}-1,3,7-trimethyl-1H-indol-6-yl)-4-[(2S)-tetrahydrofuran-2-ylmethoxy]benzamide

Base Information

Chemical Name:2-fluoro-N-(2-{[(2-hydroxy-2-methylpropyl)amino]methyl}-1,3,7-trimethyl-1H-indol-6-yl)-4-[(2S)-tetrahydrofuran-2-ylmethoxy]benzamide
CAS No.:1314127-88-2
Molecular Formula:C₂₈H₃₆FN₃O₄
Molecular Weight:497.61
Hs Code.:

Synonyms:2-fluoro-N-(2-{[(2-hydroxy-2-methylpropyl)amino]methyl}-1,3,7-trimethyl-1H-indol-6-yl)-4-[(2S)-tetrahydrofuran-2-ylmethoxy]benzamide

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Chemical Property of 2-fluoro-N-(2-{[(2-hydroxy-2-methylpropyl)amino]methyl}-1,3,7-trimethyl-1H-indol-6-yl)-4-[(2S)-tetrahydrofuran-2-ylmethoxy]benzamide

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Technology Process of 2-fluoro-N-(2-{[(2-hydroxy-2-methylpropyl)amino]methyl}-1,3,7-trimethyl-1H-indol-6-yl)-4-[(2S)-tetrahydrofuran-2-ylmethoxy]benzamide

There total 14 articles about 2-fluoro-N-(2-{[(2-hydroxy-2-methylpropyl)amino]methyl}-1,3,7-trimethyl-1H-indol-6-yl)-4-[(2S)-tetrahydrofuran-2-ylmethoxy]benzamide 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: 23.0%

: 1314129-35-5
2-fluoro-N-(2-formyl-1,3,7-trimethyl-1H-indol-6-yl)-4-[(2S)-tetrahydrofuran-2-ylmethoxy]benzamide

: 2854-16-2
1-Amino-2-methyl-propan-2-ol

: 1314127-88-2
2-fluoro-N-(2-{[(2-hydroxy-2-methylpropyl)amino]methyl}-1,3,7-trimethyl-1H-indol-6-yl)-4-[(2S)-tetrahydrofuran-2-ylmethoxy]benzamide

Guidance literature:: 2-fluoro-N-(2-formyl-1,3,7-trimethyl-1H-indol-6-yl)-4-[(2S)-tetrahydrofuran-2-ylmethoxy]benzamide; 1-Amino-2-methyl-propan-2-ol; With acetic acid; In 1-methyl-pyrrolidin-2-one; at 20 ℃; for 3h;

With sodium tris(acetoxy)borohydride; In 1-methyl-pyrrolidin-2-one; at 20 ℃; for 3h;

With sodium hydroxide; In 1-methyl-pyrrolidin-2-one; water;

Reference yield:

: 1314128-96-5
ethyl 3,7-dimethyl-6-nitro-1H-indole-2-carboxylate

: 1314127-88-2
2-fluoro-N-(2-{[(2-hydroxy-2-methylpropyl)amino]methyl}-1,3,7-trimethyl-1H-indol-6-yl)-4-[(2S)-tetrahydrofuran-2-ylmethoxy]benzamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium hydride / N,N-dimethyl-formamide; Pionier 2076 / 1.5 h / 0 - 20 °C

2.1: hydrogen / palladium-on-charcoal / ethanol; tetrahydrofuran / 12 h / 20 °C / 760.05 Torr

3.1: oxalyl dichloride / N,N-dimethyl-formamide / tetrahydrofuran / 2 h / 20 °C

3.2: 20 °C

4.1: lithium aluminium tetrahydride / tetrahydrofuran / 3 h / 0 - 20 °C

5.1: manganese(IV) oxide / tetrahydrofuran / 3 h / Reflux

6.1: acetic acid / 1-methyl-pyrrolidin-2-one / 3 h / 20 °C

6.2: 3 h / 20 °C

With manganese(IV) oxide; lithium aluminium tetrahydride; oxalyl dichloride; hydrogen; sodium hydride; acetic acid; palladium-on-charcoal; N,N-dimethyl-formamide; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; ethanol; Pionier 2076; N,N-dimethyl-formamide;

Reference yield:

: 1314129-23-1
ethyl 6-amino-1,3,7-trimethyl-1H-indole-2-carboxylate

: 1314127-88-2
2-fluoro-N-(2-{[(2-hydroxy-2-methylpropyl)amino]methyl}-1,3,7-trimethyl-1H-indol-6-yl)-4-[(2S)-tetrahydrofuran-2-ylmethoxy]benzamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: oxalyl dichloride / N,N-dimethyl-formamide / tetrahydrofuran / 2 h / 20 °C

1.2: 20 °C

2.1: lithium aluminium tetrahydride / tetrahydrofuran / 3 h / 0 - 20 °C

3.1: manganese(IV) oxide / tetrahydrofuran / 3 h / Reflux

4.1: acetic acid / 1-methyl-pyrrolidin-2-one / 3 h / 20 °C

4.2: 3 h / 20 °C

With manganese(IV) oxide; lithium aluminium tetrahydride; oxalyl dichloride; acetic acid; N,N-dimethyl-formamide; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one;