6-[4-(4-acetylpiperazin-1-yl)-2-methoxyphenyl]-3-cyclohexyl[1,2]thiazolo[5,4-d]pyrimidin-4(5H)-one

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Chemical Name:6-[4-(4-acetylpiperazin-1-yl)-2-methoxyphenyl]-3-cyclohexyl[1,2]thiazolo[5,4-d]pyrimidin-4(5H)-one
CAS No.:1374858-33-9
Molecular Formula:C₂₄H₂₉N₅O₃S
Molecular Weight:467.592
Hs Code.:

Synonyms:6-[4-(4-acetylpiperazin-1-yl)-2-methoxyphenyl]-3-cyclohexyl[1,2]thiazolo[5,4-d]pyrimidin-4(5H)-one

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Chemical Property of 6-[4-(4-acetylpiperazin-1-yl)-2-methoxyphenyl]-3-cyclohexyl[1,2]thiazolo[5,4-d]pyrimidin-4(5H)-one

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Technology Process of 6-[4-(4-acetylpiperazin-1-yl)-2-methoxyphenyl]-3-cyclohexyl[1,2]thiazolo[5,4-d]pyrimidin-4(5H)-one

There total 9 articles about 6-[4-(4-acetylpiperazin-1-yl)-2-methoxyphenyl]-3-cyclohexyl[1,2]thiazolo[5,4-d]pyrimidin-4(5H)-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: 59.0%

: 1374858-24-8
3-cyclohexyl-6-[2-methoxy-4-(piperazin-1-yl)phenyl][1,2]thiazolo[5,4-d]pyrimidin-4(5H)-one

: 75-36-5
acetyl chloride

: 1374858-33-9
6-[4-(4-acetylpiperazin-1-yl)-2-methoxyphenyl]-3-cyclohexyl[1,2]thiazolo[5,4-d]pyrimidin-4(5H)-one

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 2h;
DOI:10.1016/j.bmcl.2012.03.025

Reference yield:

: 553672-03-0
[cyclohexyl(hydroxy)methylidene]propanedinitrile

: 1374858-33-9
6-[4-(4-acetylpiperazin-1-yl)-2-methoxyphenyl]-3-cyclohexyl[1,2]thiazolo[5,4-d]pyrimidin-4(5H)-one

Guidance literature:: Multi-step reaction with 8 steps

1: trichlorophosphate / Reflux

2: ammonium hydroxide / 0.5 h / 20 °C

3: hydrogen sulfide; triethylamine / benzene

4: dihydrogen peroxide / methanol / 50 °C

5: sulfuric acid / 0.5 h / 80 °C

6: N,N-dimethyl acetamide / 0.5 h / 130 °C

7: hydrogenchloride / ethyl acetate / 2 h / 20 °C

8: triethylamine / dichloromethane / 2 h / 20 °C

With hydrogenchloride; ammonium hydroxide; sulfuric acid; hydrogen sulfide; dihydrogen peroxide; triethylamine; trichlorophosphate; In methanol; dichloromethane; N,N-dimethyl acetamide; ethyl acetate; benzene;
DOI:10.1016/j.bmcl.2012.03.025

Reference yield:

: [chloro(cyclohexyl)methylidene]propanedinitrile

: 1374858-33-9
6-[4-(4-acetylpiperazin-1-yl)-2-methoxyphenyl]-3-cyclohexyl[1,2]thiazolo[5,4-d]pyrimidin-4(5H)-one

Guidance literature:: Multi-step reaction with 7 steps

1: ammonium hydroxide / 0.5 h / 20 °C

2: hydrogen sulfide; triethylamine / benzene

3: dihydrogen peroxide / methanol / 50 °C

4: sulfuric acid / 0.5 h / 80 °C

5: N,N-dimethyl acetamide / 0.5 h / 130 °C

6: hydrogenchloride / ethyl acetate / 2 h / 20 °C

7: triethylamine / dichloromethane / 2 h / 20 °C

With hydrogenchloride; ammonium hydroxide; sulfuric acid; hydrogen sulfide; dihydrogen peroxide; triethylamine; In methanol; dichloromethane; N,N-dimethyl acetamide; ethyl acetate; benzene;
DOI:10.1016/j.bmcl.2012.03.025