1-[1-cyclohexyl-5-(4-methanesulfonyl-phenyl)-1H-pyrazol-3-yl]-4-nitrooxy-butan-1-one

Base Information

Chemical Name:1-[1-cyclohexyl-5-(4-methanesulfonyl-phenyl)-1H-pyrazol-3-yl]-4-nitrooxy-butan-1-one
CAS No.:640727-95-3
Molecular Formula:C₂₀H₂₅N₃O₆S
Molecular Weight:435.501
Hs Code.:

1-[1-cyclohexyl-5-(4-methanesulfonyl-phenyl)-1<i>H</i>-pyrazol-3-yl]-4-nitrooxy-butan-1-one

Synonyms:1-[1-cyclohexyl-5-(4-methanesulfonyl-phenyl)-1H-pyrazol-3-yl]-4-nitrooxy-butan-1-one

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Chemical Property of 1-[1-cyclohexyl-5-(4-methanesulfonyl-phenyl)-1H-pyrazol-3-yl]-4-nitrooxy-butan-1-one

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Technology Process of 1-[1-cyclohexyl-5-(4-methanesulfonyl-phenyl)-1H-pyrazol-3-yl]-4-nitrooxy-butan-1-one

There total 7 articles about 1-[1-cyclohexyl-5-(4-methanesulfonyl-phenyl)-1H-pyrazol-3-yl]-4-nitrooxy-butan-1-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: 74.0%

: 640727-94-2
1-[1-cyclohexyl-5-(4-methanesulfonyl-phenyl)-1H-pyrazol-3-yl]-4-hydroxy-butan-1-one

: 640727-95-3
1-[1-cyclohexyl-5-(4-methanesulfonyl-phenyl)-1H-pyrazol-3-yl]-4-nitrooxy-butan-1-one

Guidance literature:: With nitric acid; acetic anhydride; In chloroform; at -10 ℃;
DOI:10.1021/jm030276s

Reference yield:

: 1778-09-2
4-(Methylthio)acetophenone

: 640727-95-3
1-[1-cyclohexyl-5-(4-methanesulfonyl-phenyl)-1H-pyrazol-3-yl]-4-nitrooxy-butan-1-one

Guidance literature:: Multi-step reaction with 7 steps

1.1: 79 percent / sodium methoxide / toluene / 2 h / 20 °C

2.1: 47 percent / aq. Oxone(R) / methanol; CH₂Cl₂ / 1 h / 0 - 20 °C

3.1: 88 percent / methanol / 70 °C

4.1: trimethylaluminum / hexane; CH₂Cl₂ / 1.42 h / 0 - 20 °C

4.2: 67 percent / hexane; CH₂Cl₂ / 2 h / 20 °C

5.1: 98 percent / tetrahydrofuran / 0 - 20 °C

6.1: 79 percent / tetrabutylammonium fluoride / tetrahydrofuran / 5 h / 0 - 20 °C

7.1: 74 percent / aq. HNO₃; Ac₂O / CHCl₃ / -10 °C

With oxone; tetrabutyl ammonium fluoride; trimethylaluminum; nitric acid; sodium methylate; acetic anhydride; In tetrahydrofuran; methanol; hexane; dichloromethane; chloroform; toluene;
DOI:10.1021/jm030276s

Reference yield:

: 346684-15-9
methyl (2Z)-2-hydroxy-4-(4-methylthiophenyl)-4-oxobut-2-enoate

: 640727-95-3
1-[1-cyclohexyl-5-(4-methanesulfonyl-phenyl)-1H-pyrazol-3-yl]-4-nitrooxy-butan-1-one

Guidance literature:: Multi-step reaction with 6 steps

1.1: 47 percent / aq. Oxone(R) / methanol; CH₂Cl₂ / 1 h / 0 - 20 °C

2.1: 88 percent / methanol / 70 °C

3.1: trimethylaluminum / hexane; CH₂Cl₂ / 1.42 h / 0 - 20 °C

3.2: 67 percent / hexane; CH₂Cl₂ / 2 h / 20 °C

4.1: 98 percent / tetrahydrofuran / 0 - 20 °C

5.1: 79 percent / tetrabutylammonium fluoride / tetrahydrofuran / 5 h / 0 - 20 °C

6.1: 74 percent / aq. HNO₃; Ac₂O / CHCl₃ / -10 °C

With oxone; tetrabutyl ammonium fluoride; trimethylaluminum; nitric acid; acetic anhydride; In tetrahydrofuran; methanol; hexane; dichloromethane; chloroform;
DOI:10.1021/jm030276s