(R)-tert-butyl 8-(6-methoxy-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-ylamino)-2-phenyl-2,3-dihydropyrido[3,2-f][1,4]oxazepine-4(5H)-carboxylate

Base Information

Chemical Name:(R)-tert-butyl 8-(6-methoxy-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-ylamino)-2-phenyl-2,3-dihydropyrido[3,2-f][1,4]oxazepine-4(5H)-carboxylate
CAS No.:1255701-88-2
Molecular Formula:C₂₉H₃₂N₆O₄
Molecular Weight:528.611
Hs Code.:

Synonyms:(R)-tert-butyl 8-(6-methoxy-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-ylamino)-2-phenyl-2,3-dihydropyrido[3,2-f][1,4]oxazepine-4(5H)-carboxylate

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Chemical Property of (R)-tert-butyl 8-(6-methoxy-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-ylamino)-2-phenyl-2,3-dihydropyrido[3,2-f][1,4]oxazepine-4(5H)-carboxylate

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Technology Process of (R)-tert-butyl 8-(6-methoxy-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-ylamino)-2-phenyl-2,3-dihydropyrido[3,2-f][1,4]oxazepine-4(5H)-carboxylate

There total 7 articles about (R)-tert-butyl 8-(6-methoxy-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-ylamino)-2-phenyl-2,3-dihydropyrido[3,2-f][1,4]oxazepine-4(5H)-carboxylate 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:

: 1239719-83-5
6-methoxy-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-amine

: 1255701-86-0
(R)-tert-butyl 8-chloro-2-phenyl-2,3-dihydropyrido[3,2-f][1,4]oxazepine-4(5H)-carboxylate

: 1255701-88-2
(R)-tert-butyl 8-(6-methoxy-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-ylamino)-2-phenyl-2,3-dihydropyrido[3,2-f][1,4]oxazepine-4(5H)-carboxylate

Guidance literature:: With ethanol; caesium carbonate; acetato(2'-di-tert-butylphosphino-1,1'-biphenyl-2-yl)-palladium; In 1,2-dimethoxyethane; at 100 ℃; for 0.75h; Microwave vial; Inert atmosphere;

Reference yield:

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

: 1255701-88-2
(R)-tert-butyl 8-(6-methoxy-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-ylamino)-2-phenyl-2,3-dihydropyrido[3,2-f][1,4]oxazepine-4(5H)-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

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

2: sodium hydride / tetrahydrofuran; mineral oil / 0 - 20 °C

3: dichloromethane / 20 °C

4: ethanol; caesium carbonate / acetato(2'-di-tert-butylphosphino-1,1'-biphenyl-2-yl)-palladium / 1,2-dimethoxyethane / 0.75 h / 100 °C / Microwave vial; Inert atmosphere

With ethanol; sodium hydride; caesium carbonate; N-ethyl-N,N-diisopropylamine; acetato(2'-di-tert-butylphosphino-1,1'-biphenyl-2-yl)-palladium; In tetrahydrofuran; 1,2-dimethoxyethane; dichloromethane; N,N-dimethyl-formamide; mineral oil;

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 1255701-88-2
(R)-tert-butyl 8-(6-methoxy-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-ylamino)-2-phenyl-2,3-dihydropyrido[3,2-f][1,4]oxazepine-4(5H)-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: dichloromethane / 20 °C

2: ethanol; caesium carbonate / acetato(2'-di-tert-butylphosphino-1,1'-biphenyl-2-yl)-palladium / 1,2-dimethoxyethane / 0.75 h / 100 °C / Microwave vial; Inert atmosphere

With ethanol; caesium carbonate; acetato(2'-di-tert-butylphosphino-1,1'-biphenyl-2-yl)-palladium; In 1,2-dimethoxyethane; dichloromethane;