(+)-(3S,4R,5Z)-2-methyl-6-[(S)-N-methyl-S-phenylsulfonimidoyl]-4-phenyl-5-hexen-3-yl carbamate

Base Information

Chemical Name:(+)-(3S,4R,5Z)-2-methyl-6-[(S)-N-methyl-S-phenylsulfonimidoyl]-4-phenyl-5-hexen-3-yl carbamate
CAS No.:573681-06-8
Molecular Formula:C₂₁H₂₆N₂O₃S
Molecular Weight:386.515
Hs Code.:

Synonyms:(+)-(3S,4R,5Z)-2-methyl-6-[(S)-N-methyl-S-phenylsulfonimidoyl]-4-phenyl-5-hexen-3-yl carbamate

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Chemical Property of (+)-(3S,4R,5Z)-2-methyl-6-[(S)-N-methyl-S-phenylsulfonimidoyl]-4-phenyl-5-hexen-3-yl carbamate

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Technology Process of (+)-(3S,4R,5Z)-2-methyl-6-[(S)-N-methyl-S-phenylsulfonimidoyl]-4-phenyl-5-hexen-3-yl carbamate

There total 1 articles about (+)-(3S,4R,5Z)-2-methyl-6-[(S)-N-methyl-S-phenylsulfonimidoyl]-4-phenyl-5-hexen-3-yl carbamate 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: 76.0%

: 573680-95-2
C₂₀H₂₅NO₂S

: 3019-71-4
Trichloroacetyl isocyanate

: 573681-06-8
(+)-(3S,4R,5Z)-2-methyl-6-[(S)-N-methyl-S-phenylsulfonimidoyl]-4-phenyl-5-hexen-3-yl carbamate

: (+)-(3S,4R,5E)-2-methyl-6-[(S)-N-methyl-S-phenylsulfonimidoyl]-4-phenyl-5-hexen-3-yl carbamate

Guidance literature:: C₂₀H₂₅NO₂S; Trichloroacetyl isocyanate; In tetrahydrofuran; at 20 ℃; for 2h;

With ammonium hydroxide; at 20 ℃; for 1h;
DOI:10.1002/ejoc.200390210

Reference yield: 83.0%

: 573681-06-8
(+)-(3S,4R,5Z)-2-methyl-6-[(S)-N-methyl-S-phenylsulfonimidoyl]-4-phenyl-5-hexen-3-yl carbamate

: 159951-03-8
C₆H₅C₁₀H₁₂SON

: (+)-(4S,5R,6S)-tetrahydro-6-(1-methylethyl)-4-{[(S)-N-methyl-S-phenylsulfonimidoyl]methyl}-5-phenyl-2H-1,3-oxazin-2-one

Guidance literature:: With n-butyllithium; In tetrahydrofuran; hexane; at -78 - 20 ℃; for 18h;
DOI:10.1002/ejoc.200390210

Reference yield:

: 573681-06-8
(+)-(3S,4R,5Z)-2-methyl-6-[(S)-N-methyl-S-phenylsulfonimidoyl]-4-phenyl-5-hexen-3-yl carbamate

: 1193-82-4,4850-71-9,18453-46-8,20696-08-6
(S)-methylphenylsulfoxide

Guidance literature:: Multi-step reaction with 3 steps

1: 83 percent / nBuLi / tetrahydrofuran; hexane / 18 h / -78 - 20 °C

2: 75 percent / CH₂Cl₂ / 20 °C

3: 70 percent / tetrahydrofuran / 0.75 h / -78 °C

With n-butyllithium; In tetrahydrofuran; hexane; dichloromethane;
DOI:10.1002/ejoc.200390210