2S-isobutyl-3-(4-(methylsulfonyl)phenylthio)butan-1,4-dioic acid 4-tert-butyl ester

Base Information

Chemical Name:2S-isobutyl-3-(4-(methylsulfonyl)phenylthio)butan-1,4-dioic acid 4-tert-butyl ester
CAS No.:198421-63-5
Molecular Formula:C₁₉H₂₈O₆S₂
Molecular Weight:416.56
Hs Code.:

Synonyms:2S-isobutyl-3-(4-(methylsulfonyl)phenylthio)butan-1,4-dioic acid 4-tert-butyl ester

Suppliers and Price of 2S-isobutyl-3-(4-(methylsulfonyl)phenylthio)butan-1,4-dioic acid 4-tert-butyl ester

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 2S-isobutyl-3-(4-(methylsulfonyl)phenylthio)butan-1,4-dioic acid 4-tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2S-isobutyl-3-(4-(methylsulfonyl)phenylthio)butan-1,4-dioic acid 4-tert-butyl ester

There total 1 articles about 2S-isobutyl-3-(4-(methylsulfonyl)phenylthio)butan-1,4-dioic acid 4-tert-butyl 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: 34.0%

: 92424-06-1
bis[4-(methanesulfonyl)phenyl] disulfide

: 112245-04-2
(R)-2-(2-(tert-butoxy)-2-oxoethyl)-4-methylpentanoic acid

: 198421-63-5
2S-isobutyl-3-(4-(methylsulfonyl)phenylthio)butan-1,4-dioic acid 4-tert-butyl ester

Guidance literature:: (R)-2-(2-(tert-butoxy)-2-oxoethyl)-4-methylpentanoic acid; With lithium diisopropyl amide; In tetrahydrofuran; hexane; at -78 ℃;

bis[4-(methanesulfonyl)phenyl] disulfide; In hexane; N,N-dimethyl-formamide; at -78 - 20 ℃;
DOI:10.1021/jm990377j

Reference yield: 78.0%

: 89226-12-0
(S)-2-amino-N,3,3-trimethylbutanamide

: 198421-63-5
2S-isobutyl-3-(4-(methylsulfonyl)phenylthio)butan-1,4-dioic acid 4-tert-butyl ester

: 198421-64-6
N²-[4-tert-butyloxy-2S-isobutyl-3-(4-(methylsulfonyl)phenylthio)succinyl]-L-tert-leucine-N¹-methylamide

Guidance literature:: With dmap; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1021/jm990377j

Reference yield:

: 198421-63-5
2S-isobutyl-3-(4-(methylsulfonyl)phenylthio)butan-1,4-dioic acid 4-tert-butyl ester

: 198421-62-4
N²-[4-hydroxy-2S-isobutyl-3-(4-(methylsulfonyl)phenylthio)succinyl]-L-tert-leucine-N¹-methylamide

Guidance literature:: Multi-step reaction with 2 steps

1: 78 percent / HOBT; N-ethyl-N'-(3-dimethylaminopropyl)carbodiimide hydrochloride; DMAP / dimethylformamide / 20 °C

2: 73 percent / TFA / CH₂Cl₂ / 18 h / 0 °C

With dmap; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; trifluoroacetic acid; In dichloromethane; N,N-dimethyl-formamide; 1: Condensation / 2: acidolysis;
DOI:10.1021/jm990377j