4-chloro-6-phenethyl-6,7-dihydro-5H-pyrimido[4,5-e][1,4]diazepin-8(9H)-one

Base Information

Chemical Name:4-chloro-6-phenethyl-6,7-dihydro-5H-pyrimido[4,5-e][1,4]diazepin-8(9H)-one
CAS No.:1341216-99-6
Molecular Formula:C₁₅H₁₅ClN₄O
Molecular Weight:302.763
Hs Code.:

Synonyms:4-chloro-6-phenethyl-6,7-dihydro-5H-pyrimido[4,5-e][1,4]diazepin-8(9H)-one

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Chemical Property of 4-chloro-6-phenethyl-6,7-dihydro-5H-pyrimido[4,5-e][1,4]diazepin-8(9H)-one

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Technology Process of 4-chloro-6-phenethyl-6,7-dihydro-5H-pyrimido[4,5-e][1,4]diazepin-8(9H)-one

There total 3 articles about 4-chloro-6-phenethyl-6,7-dihydro-5H-pyrimido[4,5-e][1,4]diazepin-8(9H)-one 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: 77.0%

: 1341216-84-9
ethyl 2-(((4-amino-6-chloropyrimidin-5-yl)methyl)(phenethyl)amino)acetate

: 1341216-99-6
4-chloro-6-phenethyl-6,7-dihydro-5H-pyrimido[4,5-e][1,4]diazepin-8(9H)-one

Guidance literature:: With sodium hydride; In tetrahydrofuran; mineral oil; at 0 - 20 ℃; Inert atmosphere;
DOI:10.1002/jhet.615

Reference yield:

: 1341216-79-2
(4-amino-6-chloropyrimidin-5-yl)methanol

: 1341216-99-6
4-chloro-6-phenethyl-6,7-dihydro-5H-pyrimido[4,5-e][1,4]diazepin-8(9H)-one

Guidance literature:: Multi-step reaction with 3 steps

1: thionyl chloride / dichloromethane / 0.17 h / 0 - 20 °C

2: N-ethyl-N,N-diisopropylamine / acetonitrile / 0 - 20 °C

3: sodium hydride / tetrahydrofuran; mineral oil / 0 - 20 °C / Inert atmosphere

With thionyl chloride; sodium hydride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; acetonitrile; mineral oil;
DOI:10.1002/jhet.615

Reference yield:

: 14160-93-1
4-amino-6-chloro-pyrimidine-5-carbaldehyde

: 1341216-99-6
4-chloro-6-phenethyl-6,7-dihydro-5H-pyrimido[4,5-e][1,4]diazepin-8(9H)-one

Guidance literature:: Multi-step reaction with 4 steps

1: sodium tetrahydroborate / methanol / 0.17 h / 0 - 20 °C

2: thionyl chloride / dichloromethane / 0.17 h / 0 - 20 °C

3: N-ethyl-N,N-diisopropylamine / acetonitrile / 0 - 20 °C

4: sodium hydride / tetrahydrofuran; mineral oil / 0 - 20 °C / Inert atmosphere

With sodium tetrahydroborate; thionyl chloride; sodium hydride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; dichloromethane; acetonitrile; mineral oil;
DOI:10.1002/jhet.615