C₂₃H₃₃N₅O₄S

Base Information

Chemical Name:C₂₃H₃₃N₅O₄S
CAS No.:99701-50-5
Molecular Formula:C₂₃H₃₃N₅O₄S
Molecular Weight:475.612
Hs Code.:

C<sub>23</sub>H<sub>33</sub>N<sub>5</sub>O<sub>4</sub>S

Synonyms:C₂₃H₃₃N₅O₄S

Suppliers and Price of C₂₃H₃₃N₅O₄S

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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 C₂₃H₃₃N₅O₄S

Chemical Property:

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Technology Process of C₂₃H₃₃N₅O₄S

There total 4 articles about C₂₃H₃₃N₅O₄S 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: 75.0%

: 420-04-2
CYANAMID

: 99701-27-6
CHS-Met-Leu-Phe-OMe

: 99701-50-5
C₂₃H₃₃N₅O₄S

Guidance literature:: With mercury(II) diacetate; triethylamine; In acetonitrile;
DOI:10.1139/v85-511

Reference yield:

: 77543-00-1,65929-03-5
N-formylmethionylleucylphenylalanine methyl ester

: 99701-50-5
C₂₃H₃₃N₅O₄S

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / thionation reagent (prepared from diphenyl ether and phosphorus pentasulfide) / tetrahydrofuran / 1 h / 0 °C

2: 75 percent / triethylamine, mercuric acetate / acetonitrile

With thionation reagent (prepared from diphenyl ether and phosphorus pentasulfide); mercury(II) diacetate; triethylamine; In tetrahydrofuran; acetonitrile;
DOI:10.1139/v85-511

Reference yield:

: 77542-78-0
Boc-Met-Leu-Phe-OMe

: 99701-50-5
C₂₃H₃₃N₅O₄S

Guidance literature:: Multi-step reaction with 4 steps

1: 98percent formic acid / 3 h / Ambient temperature

2: EEDQ / CHCl₃ / 8 h / Ambient temperature

3: 70 percent / thionation reagent (prepared from diphenyl ether and phosphorus pentasulfide) / tetrahydrofuran / 1 h / 0 °C

4: 75 percent / triethylamine, mercuric acetate / acetonitrile

With formic acid; thionation reagent (prepared from diphenyl ether and phosphorus pentasulfide); mercury(II) diacetate; N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; triethylamine; In tetrahydrofuran; chloroform; acetonitrile;
DOI:10.1139/v85-511