(4S,2E)-2-methyl-5-phenyl-4-[N-(2,4,6-trimethylphenylsulfonyl)amino]-O-methylsulfonylpent-2-en-1-ol

Base Information

• Chemical Name: (4S,2E)-2-methyl-5-phenyl-4-[N-(2,4,6-trimethylphenylsulfonyl)amino]-O-methylsulfonylpent-2-en-1-ol
• CAS No.: 678166-52-4
• Molecular Formula: C₂₂H₂₉NO₅S₂
• Molecular Weight: 451.608
• Mol file: 678166-52-4.mol

Synonyms:(4S,2E)-2-methyl-5-phenyl-4-[N-(2,4,6-trimethylphenylsulfonyl)amino]-O-methylsulfonylpent-2-en-1-ol

Chemical Property of (4S,2E)-2-methyl-5-phenyl-4-[N-(2,4,6-trimethylphenylsulfonyl)amino]-O-methylsulfonylpent-2-en-1-ol

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (4S,2E)-2-methyl-5-phenyl-4-[N-(2,4,6-trimethylphenylsulfonyl)amino]-O-methylsulfonylpent-2-en-1-ol

There total 4 articles about (4S,2E)-2-methyl-5-phenyl-4-[N-(2,4,6-trimethylphenylsulfonyl)amino]-O-methylsulfonylpent-2-en-1-ol 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: 83.0%

methanesulfonyl chloride (124-63-0) + (4S,2E)-2-methyl-5-phenyl-4-[N-(2,4,6-trimethylphenylsulfonyl)amino]pent-2-en-1-ol (678166-33-1) → (4S,2E)-2-methyl-5-phenyl-4-[N-(2,4,6-trimethylphenylsulfonyl)amino]-O-methylsulfonylpent-2-en-1-ol (678166-52-4)

Guidance literature:

With triethylamine; In tetrahydrofuran; at 0 ℃; for 0.5h;

DOI:10.1248/cpb.52.111

Reference yield:

(S)-N-(2,4,6-trimethylphenylsulfonyl)phenylalaninol (182880-90-6) → (4S,2E)-2-methyl-5-phenyl-4-[N-(2,4,6-trimethylphenylsulfonyl)amino]-O-methylsulfonylpent-2-en-1-ol (678166-52-4)

Guidance literature:

Multi-step reaction with 4 steps

1: (COCl)2; DMSO; diisopropylethylamine / CHCl₃; CH₂Cl₂ / 0.5 h / -78 °C

2: 3.56 g / CHCl₃ / 18 h / 0 °C

3: 99 percent / DIBAL-H / CHCl₃; toluene / 1 h / -78 °C

4: 83 percent / Et₃N / tetrahydrofuran / 0.5 h / 0 °C

With oxalyl dichloride; diisobutylaluminium hydride; dimethyl sulfoxide; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; chloroform; toluene; 1: Swern oxidation;

DOI:10.1248/cpb.52.111

Reference yield:

N-((S)-1-Formyl-2-phenyl-ethyl)-2,4,6-trimethyl-benzenesulfonamide (220324-31-2) → (4S,2E)-2-methyl-5-phenyl-4-[N-(2,4,6-trimethylphenylsulfonyl)amino]-O-methylsulfonylpent-2-en-1-ol (678166-52-4)

Guidance literature:

Multi-step reaction with 3 steps

1: 3.56 g / CHCl₃ / 18 h / 0 °C

2: 99 percent / DIBAL-H / CHCl₃; toluene / 1 h / -78 °C

3: 83 percent / Et₃N / tetrahydrofuran / 0.5 h / 0 °C

With diisobutylaluminium hydride; triethylamine; In tetrahydrofuran; chloroform; toluene;

DOI:10.1248/cpb.52.111

upstream raw materials:

methanesulfonyl chloride

(4S,2E)-2-methyl-5-phenyl-4-[N-(2,4,6-trimethylphenylsulfonyl)amino]pent-2-en-1-ol

(S)-N-(2,4,6-trimethylphenylsulfonyl)phenylalaninol

N-((S)-1-Formyl-2-phenyl-ethyl)-2,4,6-trimethyl-benzenesulfonamide