(4R)-4-[N-(tert-butoxycarbonyl)-N-(2,4,6-trimethyl-phenylsulfonyl)amino]-5-methyl-hexan-1-ol

Base Information

Chemical Name:(4R)-4-[N-(tert-butoxycarbonyl)-N-(2,4,6-trimethyl-phenylsulfonyl)amino]-5-methyl-hexan-1-ol
CAS No.:494755-75-8
Molecular Formula:C₂₁H₃₅NO₅S
Molecular Weight:413.579
Hs Code.:

Synonyms:(4R)-4-[N-(tert-butoxycarbonyl)-N-(2,4,6-trimethyl-phenylsulfonyl)amino]-5-methyl-hexan-1-ol

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Chemical Property of (4R)-4-[N-(tert-butoxycarbonyl)-N-(2,4,6-trimethyl-phenylsulfonyl)amino]-5-methyl-hexan-1-ol

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Technology Process of (4R)-4-[N-(tert-butoxycarbonyl)-N-(2,4,6-trimethyl-phenylsulfonyl)amino]-5-methyl-hexan-1-ol

There total 4 articles about (4R)-4-[N-(tert-butoxycarbonyl)-N-(2,4,6-trimethyl-phenylsulfonyl)amino]-5-methyl-hexan-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: 92.0%

: 494755-73-6
ethyl (4R)-4-[N-(tert-butoxycarbonyl)-N-(2,4,6-trimethyl-phenylsulfonyl)amino]-5-methyl-hexanoate

: 494755-75-8
(4R)-4-[N-(tert-butoxycarbonyl)-N-(2,4,6-trimethyl-phenylsulfonyl)amino]-5-methyl-hexan-1-ol

Guidance literature:: With diisobutylaluminium hydride; In dichloromethane; toluene; at -78 - -30 ℃; for 1.5h;
DOI:10.1021/ja0262277

Reference yield:

: 494755-72-5
ethyl (4S)-4-[N-(tert-butoxycarbonyl)amino]-5-methylhexanoate

: 494755-75-8
(4R)-4-[N-(tert-butoxycarbonyl)-N-(2,4,6-trimethyl-phenylsulfonyl)amino]-5-methyl-hexan-1-ol

Guidance literature:: Multi-step reaction with 4 steps

1: trifluoroacetic acid / CH₂Cl₂ / 1 h / 20 °C

2: 1.34 g / Et₃N / CHCl₃ / 1.5 h / 20 °C

3: 78 percent / DMAP; Et₃N / CH₂Cl₂ / 7.5 h / Heating

4: 92 percent / DIBAL-H / toluene; CH₂Cl₂ / 1.5 h / -78 - -30 °C

With dmap; diisobutylaluminium hydride; triethylamine; trifluoroacetic acid; In dichloromethane; chloroform; toluene;
DOI:10.1021/ja0262277

Reference yield:

: 494755-74-7
(R)-5-Methyl-4-(2,4,6-trimethyl-benzenesulfonylamino)-hexanoic acid ethyl ester

: 494755-75-8
(4R)-4-[N-(tert-butoxycarbonyl)-N-(2,4,6-trimethyl-phenylsulfonyl)amino]-5-methyl-hexan-1-ol

Guidance literature:: Multi-step reaction with 2 steps

1: 78 percent / DMAP; Et₃N / CH₂Cl₂ / 7.5 h / Heating

2: 92 percent / DIBAL-H / toluene; CH₂Cl₂ / 1.5 h / -78 - -30 °C

With dmap; diisobutylaluminium hydride; triethylamine; In dichloromethane; toluene;
DOI:10.1021/ja0262277