6-chloro-5-(2-chloroethyl)-N-[(4-methoxyphenyl)methyl]-2-morpholinopyrimidin-4-amine

Base Information

• Chemical Name: 6-chloro-5-(2-chloroethyl)-N-[(4-methoxyphenyl)methyl]-2-morpholinopyrimidin-4-amine
• CAS No.: 1007215-39-5
• Molecular Formula: C₁₈H₂₂Cl₂N₄O₂
• Molecular Weight: 397.304
• Mol file: 1007215-39-5.mol

Synonyms:6-chloro-5-(2-chloroethyl)-N-[(4-methoxyphenyl)methyl]-2-morpholinopyrimidin-4-amine

Chemical Property of 6-chloro-5-(2-chloroethyl)-N-[(4-methoxyphenyl)methyl]-2-morpholinopyrimidin-4-amine

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 6-chloro-5-(2-chloroethyl)-N-[(4-methoxyphenyl)methyl]-2-morpholinopyrimidin-4-amine

There total 4 articles about 6-chloro-5-(2-chloroethyl)-N-[(4-methoxyphenyl)methyl]-2-morpholinopyrimidin-4-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: 68.0%

4-[4,6-dichloro-5-(2-chloroethyl)-pyrimidin-2-yl]-morpholine (1007206-27-0) + 4-methoxy-benzylamine (2393-23-9) → 6-chloro-5-(2-chloroethyl)-N-[(4-methoxyphenyl)methyl]-2-morpholinopyrimidin-4-amine (1007215-39-5)

Guidance literature:

With N-ethyl-N,N-diisopropylamine; In acetonitrile; for 17h; Reflux;

DOI:10.1016/j.bmc.2015.11.009

Reference yield:

2-oxotetrahydrofuran-3-carboxylic acid methyl ester (127915-15-5,19406-00-9) → 6-chloro-5-(2-chloroethyl)-N-[(4-methoxyphenyl)methyl]-2-morpholinopyrimidin-4-amine (1007215-39-5)

Guidance literature:

Multi-step reaction with 3 steps

1: sodium / methanol / 2 h / Reflux

2: trichlorophosphate / 10 h / 100 °C

3: N-ethyl-N,N-diisopropylamine / acetonitrile / 17 h / Reflux

With sodium; N-ethyl-N,N-diisopropylamine; trichlorophosphate; In methanol; acetonitrile;

DOI:10.1016/j.bmc.2015.11.009

Reference yield:

morpholinoformamidine hydrochloride (5638-78-8) → 6-chloro-5-(2-chloroethyl)-N-[(4-methoxyphenyl)methyl]-2-morpholinopyrimidin-4-amine (1007215-39-5)

Guidance literature:

Multi-step reaction with 3 steps

1: sodium / methanol / 2 h / Reflux

2: trichlorophosphate / 10 h / 100 °C

3: N-ethyl-N,N-diisopropylamine / acetonitrile / 17 h / Reflux

With sodium; N-ethyl-N,N-diisopropylamine; trichlorophosphate; In methanol; acetonitrile;

DOI:10.1016/j.bmc.2015.11.009

upstream raw materials:

4-[4,6-dichloro-5-(2-chloroethyl)-pyrimidin-2-yl]-morpholine

4-methoxy-benzylamine

2-oxotetrahydrofuran-3-carboxylic acid methyl ester

morpholinoformamidine hydrochloride

Downstream raw materials:

4-[4-chloro-7-[(4-methoxyphenyl)methyl]-5,6-dihydropyrrolo[2,3-d]pyrimidin-2-yl]morpholine

1-[4-[2-[bis[(4-methoxyphenyl)methyl]amino]pyrimidin-5-yl]-2-morpholino-5,6-dihydro-pyrrolo[2,3-d]pyrimidin-7-yl]ethanone

[3-[4-(2-aminopyrimidin-5-yl)-2-morpholino-5,6-dihydropyrrolo[2,3-d]pyrimidin-7-yl]phenyl]-(4-methylpiperazin-1-yl)methanone

N,N-bis[(4-methoxyphenyl)methyl]-5-(2-morpholino-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)pyrimidin-2-amine