3β-acetoxy-20-[5-(1-hydroxy-1-methylethyl)isoxazol-3-yl]-5α,8α-(3,5-dioxo-4-phenyl-1,2,4-triazolidino)pregn-6-ene

Base Information

Chemical Name:3β-acetoxy-20-[5-(1-hydroxy-1-methylethyl)isoxazol-3-yl]-5α,8α-(3,5-dioxo-4-phenyl-1,2,4-triazolidino)pregn-6-ene
CAS No.:212248-27-6
Molecular Formula:C₃₇H₄₆N₄O₆
Molecular Weight:642.795
Hs Code.:

Synonyms:3β-acetoxy-20-[5-(1-hydroxy-1-methylethyl)isoxazol-3-yl]-5α,8α-(3,5-dioxo-4-phenyl-1,2,4-triazolidino)pregn-6-ene

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Chemical Property of 3β-acetoxy-20-[5-(1-hydroxy-1-methylethyl)isoxazol-3-yl]-5α,8α-(3,5-dioxo-4-phenyl-1,2,4-triazolidino)pregn-6-ene

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Technology Process of 3β-acetoxy-20-[5-(1-hydroxy-1-methylethyl)isoxazol-3-yl]-5α,8α-(3,5-dioxo-4-phenyl-1,2,4-triazolidino)pregn-6-ene

There total 6 articles about 3β-acetoxy-20-[5-(1-hydroxy-1-methylethyl)isoxazol-3-yl]-5α,8α-(3,5-dioxo-4-phenyl-1,2,4-triazolidino)pregn-6-ene 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:

: 15988-11-1
4-Phenylurazole

: 212248-27-6
3β-acetoxy-20-[5-(1-hydroxy-1-methylethyl)isoxazol-3-yl]-5α,8α-(3,5-dioxo-4-phenyl-1,2,4-triazolidino)pregn-6-ene

Guidance literature:: Multi-step reaction with 5 steps

1: 1.) NBS, 2.) pyridine / 1.) EtOAc, 10 min, 2.) EtOAc, r.t., 30 min

2: 1.) NaHCO₃, pyridine, O₃, 2.) Me₂S / 1.) CHCl₃, MeOH, -70 deg C, 5 min, 2.) CHCl₃, MeOH, r.t., overnight

3: 93 percent / pyridine, H₂NOH*HCl / 24 h / Ambient temperature

4: N-chlorosuccinimide, pyridine / CHCl₃ / 0.33 h

5: Et₃N / CHCl₃ / 24 h / Ambient temperature

With pyridine; N-chloro-succinimide; N-Bromosuccinimide; dimethylsulfide; hydroxylamine hydrochloride; sodium hydrogencarbonate; ozone; triethylamine; In chloroform;

Reference yield:

: 1108-03-8,2874-25-1,3957-39-9,57760-54-0,60018-28-2,78148-63-7,125225-12-9,2418-45-3
ergosterol acetate

: 212248-27-6
3β-acetoxy-20-[5-(1-hydroxy-1-methylethyl)isoxazol-3-yl]-5α,8α-(3,5-dioxo-4-phenyl-1,2,4-triazolidino)pregn-6-ene

Guidance literature:: Multi-step reaction with 5 steps

1: 1.) NBS, 2.) pyridine / 1.) EtOAc, 10 min, 2.) EtOAc, r.t., 30 min

2: 1.) NaHCO₃, pyridine, O₃, 2.) Me₂S / 1.) CHCl₃, MeOH, -70 deg C, 5 min, 2.) CHCl₃, MeOH, r.t., overnight

3: 93 percent / pyridine, H₂NOH*HCl / 24 h / Ambient temperature

4: N-chlorosuccinimide, pyridine / CHCl₃ / 0.33 h

5: Et₃N / CHCl₃ / 24 h / Ambient temperature

With pyridine; N-chloro-succinimide; N-Bromosuccinimide; dimethylsulfide; hydroxylamine hydrochloride; sodium hydrogencarbonate; ozone; triethylamine; In chloroform;

Reference yield:

: 212248-24-3
3β-acetoxy-5α,8α-(3,5-dioxo-4-phenyl-1,2,4-triazolidino)-23-norcholest-6-en-22-aldoxime

: 212248-27-6
3β-acetoxy-20-[5-(1-hydroxy-1-methylethyl)isoxazol-3-yl]-5α,8α-(3,5-dioxo-4-phenyl-1,2,4-triazolidino)pregn-6-ene

Guidance literature:: Multi-step reaction with 2 steps

1: N-chlorosuccinimide, pyridine / CHCl₃ / 0.33 h

2: Et₃N / CHCl₃ / 24 h / Ambient temperature

With pyridine; N-chloro-succinimide; triethylamine; In chloroform;