17β-acetoxy-1α-[4'-(4''-tert-butylphenyl)-1'H-1',2',3'-triazol-1'-yl]-5α-androstan-3-one

Base Information

Chemical Name:17β-acetoxy-1α-[4'-(4''-tert-butylphenyl)-1'H-1',2',3'-triazol-1'-yl]-5α-androstan-3-one
CAS No.:1350714-58-7
Molecular Formula:C₃₃H₄₅N₃O₃
Molecular Weight:531.739
Hs Code.:

Synonyms:17β-acetoxy-1α-[4'-(4''-tert-butylphenyl)-1'H-1',2',3'-triazol-1'-yl]-5α-androstan-3-one

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Chemical Property of 17β-acetoxy-1α-[4'-(4''-tert-butylphenyl)-1'H-1',2',3'-triazol-1'-yl]-5α-androstan-3-one

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Technology Process of 17β-acetoxy-1α-[4'-(4''-tert-butylphenyl)-1'H-1',2',3'-triazol-1'-yl]-5α-androstan-3-one

There total 4 articles about 17β-acetoxy-1α-[4'-(4''-tert-butylphenyl)-1'H-1',2',3'-triazol-1'-yl]-5α-androstan-3-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: 19.0%

: 1350714-36-1
17β-acetoxy-1α-[4'-(4''-tert-butylphenyl)-1'H-1',2',3'-triazol-1'-yl]-5α-androstan-3β-ol

: 1350714-58-7
17β-acetoxy-1α-[4'-(4''-tert-butylphenyl)-1'H-1',2',3'-triazol-1'-yl]-5α-androstan-3-one

: 64-82-4,6656-41-3,21507-42-6,25615-33-2,54631-35-5,79732-37-9,97413-69-9
(5α,17β)-3-oxoandrost-1-en-17-yl acetate

Guidance literature:: With Jones reagent; In acetone; at 20 ℃; for 0.333333h;
DOI:10.1039/c1ob06086d

Reference yield:

: 1350714-19-0
17β-acetoxy-1α-azido-5α-androstan-3-one

: 1350714-58-7
17β-acetoxy-1α-[4'-(4''-tert-butylphenyl)-1'H-1',2',3'-triazol-1'-yl]-5α-androstan-3-one

Guidance literature:: Multi-step reaction with 3 steps

1: potassium borohydride; acetic acid / methanol / 3 h / pH 6 - 8

2: copper(l) iodide; N-ethyl-N,N-diisopropylamine; triphenylphosphine / toluene / 3 h / 111 °C

3: Jones reagent / acetone / 0.33 h / 20 °C

With copper(l) iodide; Jones reagent; potassium borohydride; acetic acid; N-ethyl-N,N-diisopropylamine; triphenylphosphine; In methanol; acetone; toluene; 3: Jones oxidation;
DOI:10.1039/c1ob06086d

Reference yield:

: 1350714-20-3
17β-acetoxy-1α-azido-5α-androstan-3β-ol

: 1350714-58-7
17β-acetoxy-1α-[4'-(4''-tert-butylphenyl)-1'H-1',2',3'-triazol-1'-yl]-5α-androstan-3-one

Guidance literature:: Multi-step reaction with 2 steps

1: copper(l) iodide; N-ethyl-N,N-diisopropylamine; triphenylphosphine / toluene / 3 h / 111 °C

2: Jones reagent / acetone / 0.33 h / 20 °C

With copper(l) iodide; Jones reagent; N-ethyl-N,N-diisopropylamine; triphenylphosphine; In acetone; toluene; 2: Jones oxidation;
DOI:10.1039/c1ob06086d