(R)-N-(6-methoxy-5-(4-methyl-1H-imidazol-1-yl)pyridin-2-yl)-4-methyl-2-phenyl-2,3,4,5-tetrahydropyrido[3,2-f][1,4]oxazepin-8-amine

Base Information

Chemical Name:(R)-N-(6-methoxy-5-(4-methyl-1H-imidazol-1-yl)pyridin-2-yl)-4-methyl-2-phenyl-2,3,4,5-tetrahydropyrido[3,2-f][1,4]oxazepin-8-amine
CAS No.:1255700-28-7
Molecular Formula:C₂₅H₂₆N₆O₂
Molecular Weight:442.52
Hs Code.:

Synonyms:(R)-N-(6-methoxy-5-(4-methyl-1H-imidazol-1-yl)pyridin-2-yl)-4-methyl-2-phenyl-2,3,4,5-tetrahydropyrido[3,2-f][1,4]oxazepin-8-amine

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Chemical Property of (R)-N-(6-methoxy-5-(4-methyl-1H-imidazol-1-yl)pyridin-2-yl)-4-methyl-2-phenyl-2,3,4,5-tetrahydropyrido[3,2-f][1,4]oxazepin-8-amine

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Technology Process of (R)-N-(6-methoxy-5-(4-methyl-1H-imidazol-1-yl)pyridin-2-yl)-4-methyl-2-phenyl-2,3,4,5-tetrahydropyrido[3,2-f][1,4]oxazepin-8-amine

There total 7 articles about (R)-N-(6-methoxy-5-(4-methyl-1H-imidazol-1-yl)pyridin-2-yl)-4-methyl-2-phenyl-2,3,4,5-tetrahydropyrido[3,2-f][1,4]oxazepin-8-amine 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: 16.0%

: 1232039-16-5
6-methoxy-5-(4-methyl-1H-imidazol-1-yl)pyridin-2-amine

: 1255701-21-3
(R)-8-chloro-4-methyl-2-phenyl-2,3,4,5-tetrahydropyrido[3,2-f][1,4]oxazepine

: 1255700-28-7
(R)-N-(6-methoxy-5-(4-methyl-1H-imidazol-1-yl)pyridin-2-yl)-4-methyl-2-phenyl-2,3,4,5-tetrahydropyrido[3,2-f][1,4]oxazepin-8-amine

Guidance literature:: With caesium carbonate; palladium diacetate; CyJohnPhos; In 1,2-dimethoxyethane; at 100 ℃; for 2h; Inert atmosphere; Microwave vial;

Reference yield:

: 2549-14-6,1936-63-6
(R)-2-Amino-1-phenylethanol

: 1255700-28-7
(R)-N-(6-methoxy-5-(4-methyl-1H-imidazol-1-yl)pyridin-2-yl)-4-methyl-2-phenyl-2,3,4,5-tetrahydropyrido[3,2-f][1,4]oxazepin-8-amine

Guidance literature:: Multi-step reaction with 4 steps

1.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 16 h / 20 °C

2.1: acetic acid / tetrahydrofuran / 0.67 h

2.2: 0.67 h

3.1: sodium hydride / tetrahydrofuran; mineral oil / 20 °C / Inert atmosphere; Cooling with ice-water bath

4.1: caesium carbonate / palladium diacetate; CyJohnPhos / 1,2-dimethoxyethane / 2 h / 100 °C / Inert atmosphere; Microwave vial

With sodium hydride; caesium carbonate; acetic acid; N-ethyl-N,N-diisopropylamine; palladium diacetate; CyJohnPhos; In tetrahydrofuran; 1,2-dimethoxyethane; N,N-dimethyl-formamide; mineral oil;

Reference yield:

: 41789-37-1
2,6-dichloro-5-pyridylmethyl chloride

: 1255700-28-7
(R)-N-(6-methoxy-5-(4-methyl-1H-imidazol-1-yl)pyridin-2-yl)-4-methyl-2-phenyl-2,3,4,5-tetrahydropyrido[3,2-f][1,4]oxazepin-8-amine

Guidance literature:: Multi-step reaction with 4 steps

1.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 16 h / 20 °C

2.1: acetic acid / tetrahydrofuran / 0.67 h

2.2: 0.67 h

3.1: sodium hydride / tetrahydrofuran; mineral oil / 20 °C / Inert atmosphere; Cooling with ice-water bath

4.1: caesium carbonate / palladium diacetate; CyJohnPhos / 1,2-dimethoxyethane / 2 h / 100 °C / Inert atmosphere; Microwave vial

With sodium hydride; caesium carbonate; acetic acid; N-ethyl-N,N-diisopropylamine; palladium diacetate; CyJohnPhos; In tetrahydrofuran; 1,2-dimethoxyethane; N,N-dimethyl-formamide; mineral oil;