(3R,5S,6R)-2,3,5,6-Tetrahydro-3-(p-methoxyphenyl)-5,6-diphenyl-1,4-oxazin-2-one

Base Information

Chemical Name:(3R,5S,6R)-2,3,5,6-Tetrahydro-3-(p-methoxyphenyl)-5,6-diphenyl-1,4-oxazin-2-one
CAS No.:144744-25-2
Molecular Formula:C₂₃H₂₁NO₃
Molecular Weight:359.425
Hs Code.:

Synonyms:(3R,5S,6R)-2,3,5,6-Tetrahydro-3-(p-methoxyphenyl)-5,6-diphenyl-1,4-oxazin-2-one

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (3R,5S,6R)-2,3,5,6-Tetrahydro-3-(p-methoxyphenyl)-5,6-diphenyl-1,4-oxazin-2-one

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Technology Process of (3R,5S,6R)-2,3,5,6-Tetrahydro-3-(p-methoxyphenyl)-5,6-diphenyl-1,4-oxazin-2-one

There total 1 articles about (3R,5S,6R)-2,3,5,6-Tetrahydro-3-(p-methoxyphenyl)-5,6-diphenyl-1,4-oxazin-2-one 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:

: 23190-16-1
(1R,2S)-2-Amino-1,2-diphenylethanol

: 144744-25-2
(3R,5S,6R)-2,3,5,6-Tetrahydro-3-(p-methoxyphenyl)-5,6-diphenyl-1,4-oxazin-2-one

: 144744-26-3
(3S,5S,6R)-2,3,5,6-Tetrahydro-3-(p-methoxyphenyl)-5,6-diphenyl-1,4-oxazin-2-one

Guidance literature:: Yield given. Multistep reaction. Yields of byproduct given;
DOI:10.1021/jo00051a044

Reference yield:

: 144744-25-2
(3R,5S,6R)-2,3,5,6-Tetrahydro-3-(p-methoxyphenyl)-5,6-diphenyl-1,4-oxazin-2-one

: 24593-48-4,19789-59-4
(2S)-2-amino-2-(4-methoxyphenyl)acetic acid

: 24593-49-5,19789-59-4
D-(-)-2-(4-methoxyphenyl)glycine

Guidance literature:: With hydrogen; palladium dichloride; In tetrahydrofuran; ethanol; for 1h; under 760 Torr; Yield given. Yields of byproduct given. Title compound not separated from byproducts;
DOI:10.1021/jo00051a044