(+)-(R)-2-tert-butoxycarbonylamino-N-(2,6-dimethylphenyl)propanethioamide

Base Information

Chemical Name:(+)-(R)-2-tert-butoxycarbonylamino-N-(2,6-dimethylphenyl)propanethioamide
CAS No.:936628-29-4
Molecular Formula:C₁₆H₂₄N₂O₂S
Molecular Weight:308.445
Hs Code.:

Synonyms:(+)-(R)-2-tert-butoxycarbonylamino-N-(2,6-dimethylphenyl)propanethioamide

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Chemical Property of (+)-(R)-2-tert-butoxycarbonylamino-N-(2,6-dimethylphenyl)propanethioamide

Chemical Property:

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Technology Process of (+)-(R)-2-tert-butoxycarbonylamino-N-(2,6-dimethylphenyl)propanethioamide

There total 4 articles about (+)-(R)-2-tert-butoxycarbonylamino-N-(2,6-dimethylphenyl)propanethioamide 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: 50.0%

: 151416-30-7
(+)-(R)-N²-(tert-butoxycarbonyl)-N¹-(2,6-dimethylphenyl)alaninamide

: 936628-29-4
(+)-(R)-2-tert-butoxycarbonylamino-N-(2,6-dimethylphenyl)propanethioamide

Guidance literature:: With 2,4-bis(p-pentyloxyphenyl)dithiadiphosphethane 2,4-disulfide; In benzene; for 48h; Heating;
DOI:10.1021/jm061078e

Reference yield:

: 3744-87-4,7764-95-6,15761-38-3
Boc-(R)-Ala

: 936628-29-4
(+)-(R)-2-tert-butoxycarbonylamino-N-(2,6-dimethylphenyl)propanethioamide

Guidance literature:: Multi-step reaction with 2 steps

1: 2-isobutoxy-1-isobutoxycarbonyl-1,2-dihydroquinoline; triethylamine / CHCl₃ / 6 h / Heating

2: 50 percent / 2,4-bis(p-pentyloxyphenyl)dithiadiphosphethane 2,4-disulfide / benzene / 48 h / Heating

With 2-isobutoxy-1-isobutoxycarbonyl-1,2-dihydroquinoline; triethylamine; In chloroform; benzene;
DOI:10.1021/jm061078e

Reference yield:

: 73371-96-7
2-<<(tert-butoxycarbonyl)oxy>imino>-2-phenylacetonitrile

: 936628-29-4
(+)-(R)-2-tert-butoxycarbonylamino-N-(2,6-dimethylphenyl)propanethioamide

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / H₂O; dioxane / 20 °C

2: 2-isobutoxy-1-isobutoxycarbonyl-1,2-dihydroquinoline; triethylamine / CHCl₃ / 6 h / Heating

3: 50 percent / 2,4-bis(p-pentyloxyphenyl)dithiadiphosphethane 2,4-disulfide / benzene / 48 h / Heating

With 2-isobutoxy-1-isobutoxycarbonyl-1,2-dihydroquinoline; triethylamine; In 1,4-dioxane; chloroform; water; benzene;
DOI:10.1021/jm061078e