Carbonic acid (E)-(4S,5S)-4-(4-methoxy-2,3,6-trimethyl-benzenesulfonylamino)-5-methyl-hept-2-enyl ester methyl ester

Base Information

Chemical Name:Carbonic acid (E)-(4S,5S)-4-(4-methoxy-2,3,6-trimethyl-benzenesulfonylamino)-5-methyl-hept-2-enyl ester methyl ester
CAS No.:220306-90-1
Molecular Formula:C₂₀H₃₁NO₆S
Molecular Weight:413.535
Hs Code.:

Synonyms:Carbonic acid (E)-(4S,5S)-4-(4-methoxy-2,3,6-trimethyl-benzenesulfonylamino)-5-methyl-hept-2-enyl ester methyl ester

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Chemical Property of Carbonic acid (E)-(4S,5S)-4-(4-methoxy-2,3,6-trimethyl-benzenesulfonylamino)-5-methyl-hept-2-enyl ester methyl ester

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Technology Process of Carbonic acid (E)-(4S,5S)-4-(4-methoxy-2,3,6-trimethyl-benzenesulfonylamino)-5-methyl-hept-2-enyl ester methyl ester

There total 6 articles about Carbonic acid (E)-(4S,5S)-4-(4-methoxy-2,3,6-trimethyl-benzenesulfonylamino)-5-methyl-hept-2-enyl ester methyl ester 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: 88.0%

: 79-22-1
methyl chloroformate

: 220306-89-8
N-[(E)-(S)-1-((S)-sec-Butyl)-4-hydroxy-but-2-enyl]-4-methoxy-2,3,6-trimethyl-benzenesulfonamide

: 220306-90-1
Carbonic acid (E)-(4S,5S)-4-(4-methoxy-2,3,6-trimethyl-benzenesulfonylamino)-5-methyl-hept-2-enyl ester methyl ester

Guidance literature:: With pyridine; In chloroform; at -78 - 0 ℃; for 1h;
DOI:10.1039/a806882h

Reference yield:

: 80745-07-9
4-methoxy-2,3,6-trimethylbenzenesulfonyl chloride

: 220306-90-1
Carbonic acid (E)-(4S,5S)-4-(4-methoxy-2,3,6-trimethyl-benzenesulfonylamino)-5-methyl-hept-2-enyl ester methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 80 percent / Et₃N / CHCl₃; dimethylformamide / 6 h / 0 °C

2: 1.) (COCl)2, DMSO, 2.) (i-Pr)2NEt / 1.) CHCl₃, hexane, -78 deg C, 30 min, 2.) -78 to 0 deg C, 30 min

3: CHCl₃ / 1 h / 0 - 20 °C

4: 88 percent / DIBAL / toluene; CHCl₃ / 1 h / -78 °C

5: 88 percent / pyridine / CHCl₃ / 1 h / -78 - 0 °C

With pyridine; oxalyl dichloride; diisobutylaluminium hydride; dimethyl sulfoxide; triethylamine; N-ethyl-N,N-diisopropylamine; In chloroform; N,N-dimethyl-formamide; toluene;
DOI:10.1039/a806882h

Reference yield:

: 24629-25-2
(S)-isoleucinol

: 220306-90-1
Carbonic acid (E)-(4S,5S)-4-(4-methoxy-2,3,6-trimethyl-benzenesulfonylamino)-5-methyl-hept-2-enyl ester methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 80 percent / Et₃N / CHCl₃; dimethylformamide / 6 h / 0 °C

2: 1.) (COCl)2, DMSO, 2.) (i-Pr)2NEt / 1.) CHCl₃, hexane, -78 deg C, 30 min, 2.) -78 to 0 deg C, 30 min

3: CHCl₃ / 1 h / 0 - 20 °C

4: 88 percent / DIBAL / toluene; CHCl₃ / 1 h / -78 °C

5: 88 percent / pyridine / CHCl₃ / 1 h / -78 - 0 °C

With pyridine; oxalyl dichloride; diisobutylaluminium hydride; dimethyl sulfoxide; triethylamine; N-ethyl-N,N-diisopropylamine; In chloroform; N,N-dimethyl-formamide; toluene;
DOI:10.1039/a806882h