2-{4-[2-chloro-5-(5-isopropyl-2-methyl-phenoxymethyl)-6-methyl-pyrimidin-4-yl]-piperazin-1-yl}-acetamide

Base Information

Chemical Name:2-{4-[2-chloro-5-(5-isopropyl-2-methyl-phenoxymethyl)-6-methyl-pyrimidin-4-yl]-piperazin-1-yl}-acetamide
CAS No.:869891-40-7
Molecular Formula:C₂₂H₃₀ClN₅O₂
Molecular Weight:431.965
Hs Code.:

Synonyms:2-{4-[2-chloro-5-(5-isopropyl-2-methyl-phenoxymethyl)-6-methyl-pyrimidin-4-yl]-piperazin-1-yl}-acetamide

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Chemical Property of 2-{4-[2-chloro-5-(5-isopropyl-2-methyl-phenoxymethyl)-6-methyl-pyrimidin-4-yl]-piperazin-1-yl}-acetamide

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Technology Process of 2-{4-[2-chloro-5-(5-isopropyl-2-methyl-phenoxymethyl)-6-methyl-pyrimidin-4-yl]-piperazin-1-yl}-acetamide

There total 4 articles about 2-{4-[2-chloro-5-(5-isopropyl-2-methyl-phenoxymethyl)-6-methyl-pyrimidin-4-yl]-piperazin-1-yl}-acetamide 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:

: 869891-39-4
2-chloro-5-(5-isopropyl-2-methyl-phenoxymethyl)-4-methyl-6-piperazin-1-ylpyrimidine trifluoroacetic acid salt

: 683-57-8
bromo-acetic acid amide

: 869891-40-7
2-{4-[2-chloro-5-(5-isopropyl-2-methyl-phenoxymethyl)-6-methyl-pyrimidin-4-yl]-piperazin-1-yl}-acetamide

Guidance literature:: With potassium carbonate; In ISOPROPYLAMIDE; at 20 ℃; for 3h;

Reference yield:

: 626-48-2
6-Methyluracil

: 869891-40-7
2-{4-[2-chloro-5-(5-isopropyl-2-methyl-phenoxymethyl)-6-methyl-pyrimidin-4-yl]-piperazin-1-yl}-acetamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium hydroxide / water / 0.17 h / 20 °C

1.2: 3 h

2.1: tributyl-amine / trichlorophosphate / 7 h / 90 °C / Heating / reflux

3.1: potassium tert-butylate / tetrahydrofuran; ISOPROPYLAMIDE / 40.33 h / 0 - 20 °C

4.1: potassium carbonate / ISOPROPYLAMIDE / 16 h / 20 °C

5.1: dichloromethane / 0.33 h

6.1: potassium carbonate / ISOPROPYLAMIDE / 3 h / 20 °C

With sodium hydroxide; tributyl-amine; potassium tert-butylate; potassium carbonate; In tetrahydrofuran; dichloromethane; ISOPROPYLAMIDE; water; trichlorophosphate;

Reference yield:

: 147-61-5
5-hydroxymethyl-6-methyl-1H-pyrimidine-2,4-dione

: 869891-40-7
2-{4-[2-chloro-5-(5-isopropyl-2-methyl-phenoxymethyl)-6-methyl-pyrimidin-4-yl]-piperazin-1-yl}-acetamide

Guidance literature:: Multi-step reaction with 5 steps

1: tributyl-amine / trichlorophosphate / 7 h / 90 °C / Heating / reflux

2: potassium tert-butylate / tetrahydrofuran; ISOPROPYLAMIDE / 40.33 h / 0 - 20 °C

3: potassium carbonate / ISOPROPYLAMIDE / 16 h / 20 °C

4: dichloromethane / 0.33 h

5: potassium carbonate / ISOPROPYLAMIDE / 3 h / 20 °C

With tributyl-amine; potassium tert-butylate; potassium carbonate; In tetrahydrofuran; dichloromethane; ISOPROPYLAMIDE; trichlorophosphate;