tert-butyl 4-(3-methoxyphenylamino)-2-(4-methylpiperazin-1-yl)-8,9-dihydro-5H-pyrimido[4,5-d]azepine-7(6H)-carboxylate

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Chemical Name:tert-butyl 4-(3-methoxyphenylamino)-2-(4-methylpiperazin-1-yl)-8,9-dihydro-5H-pyrimido[4,5-d]azepine-7(6H)-carboxylate
CAS No.:1443153-39-6
Molecular Formula:C₂₅H₃₆N₆O₃
Molecular Weight:468.599
Hs Code.:

Synonyms:tert-butyl 4-(3-methoxyphenylamino)-2-(4-methylpiperazin-1-yl)-8,9-dihydro-5H-pyrimido[4,5-d]azepine-7(6H)-carboxylate

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Chemical Property of tert-butyl 4-(3-methoxyphenylamino)-2-(4-methylpiperazin-1-yl)-8,9-dihydro-5H-pyrimido[4,5-d]azepine-7(6H)-carboxylate

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Technology Process of tert-butyl 4-(3-methoxyphenylamino)-2-(4-methylpiperazin-1-yl)-8,9-dihydro-5H-pyrimido[4,5-d]azepine-7(6H)-carboxylate

There total 6 articles about tert-butyl 4-(3-methoxyphenylamino)-2-(4-methylpiperazin-1-yl)-8,9-dihydro-5H-pyrimido[4,5-d]azepine-7(6H)-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: 14.0%

: tert-butyl 2-(4-methylpiperazin-1-yl)-4-(trifluoromethylsulfonyloxy)-5,6,8,9-tetrahydro-3Hpyrimido[4,5-d]azepine-7(4H)-carboxylate

: 536-90-3,918666-97-4
m-Anisidine

: 1443153-39-6
tert-butyl 4-(3-methoxyphenylamino)-2-(4-methylpiperazin-1-yl)-8,9-dihydro-5H-pyrimido[4,5-d]azepine-7(6H)-carboxylate

Guidance literature:: In acetonitrile; at 20 ℃; for 24h; Inert atmosphere;
DOI:10.1016/j.ejmech.2013.02.020

Reference yield:

: 141642-82-2
5-oxo-azepane-1,4-dicarboxylic acid 1-tert-butyl ester 4-ethyl ester

: 1443153-39-6
tert-butyl 4-(3-methoxyphenylamino)-2-(4-methylpiperazin-1-yl)-8,9-dihydro-5H-pyrimido[4,5-d]azepine-7(6H)-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: sodium ethanolate / ethanol / 0 - 20 °C / Inert atmosphere

2: pyridine / dichloromethane / 1 h / 0 - 20 °C / Inert atmosphere

3: acetonitrile / 24 h / 20 °C / Inert atmosphere

With pyridine; sodium ethanolate; In ethanol; dichloromethane; acetonitrile;
DOI:10.1016/j.ejmech.2013.02.020

Reference yield:

: 1443153-29-4
tert-butyl 2-(4-methylpiperazin-1-yl)-4-oxo-5,6,8,9-tetrahydro-3H-pyrimido[4,5-d]azepine-7(4H)-carboxylate

: 1443153-39-6
tert-butyl 4-(3-methoxyphenylamino)-2-(4-methylpiperazin-1-yl)-8,9-dihydro-5H-pyrimido[4,5-d]azepine-7(6H)-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine / dichloromethane / 1 h / 0 - 20 °C / Inert atmosphere

2: acetonitrile / 24 h / 20 °C / Inert atmosphere

With pyridine; In dichloromethane; acetonitrile;
DOI:10.1016/j.ejmech.2013.02.020