C₂₁H₂₈S₂N₂O₅

Base Information

Chemical Name:C₂₁H₂₈S₂N₂O₅
CAS No.:941714-78-9
Molecular Formula:C₂₁H₂₈N₂O₅S₂
Molecular Weight:452.596
Hs Code.:

C<sub>21</sub>H<sub>28</sub>S<sub>2</sub>N<sub>2</sub>O<sub>5</sub>

Synonyms:C₂₁H₂₈S₂N₂O₅

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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 C₂₁H₂₈S₂N₂O₅

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Technology Process of C₂₁H₂₈S₂N₂O₅

There total 4 articles about C₂₁H₂₈S₂N₂O₅ 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: 92.0%

: 941714-77-8
(4R)-4-methyl-2-phenyl-4,5-dihydrothiazole-4-carboxylic acid

: 890534-08-4
N-Boc-methylcysteine methyl ester

: 941714-78-9
C₂₁H₂₈S₂N₂O₅

Guidance literature:: With bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; triethylamine; In dichloromethane; at 20 ℃;
DOI:10.1002/chem.200601446

Reference yield:

: C₁₆H₂₁SNO₅

: 941714-78-9
C₂₁H₂₈S₂N₂O₅

Guidance literature:: Multi-step reaction with 14 steps

1: TFA / 0.33 h / 20 °C

2: 1.64 g / benzene / 4 h / Heating

3: 92 percent / BOP-Cl; Et₃N / CH₂Cl₂ / 20 °C

4: TFA / 0.33 h / 20 °C

5: benzene / 4 h / Heating

6: 100 percent / aq. LiOH / tetrahydrofuran / 0.5 h / 20 °C

7: BOP-Cl; Et₃N / CH₂Cl₂ / 20 °C

8: TFA / 0.33 h / 20 °C

9: benzene / 4 h / Heating

10: 99 percent / aq. LiOH / tetrahydrofuran / 0.5 h / 20 °C

11: BOP-Cl; Et₃N / CH₂Cl₂ / 20 °C

12: TFA / 0.33 h / 20 °C

13: benzene / 4 h / Heating

14: 100 percent / tetrahydrofuran; methanol / 20 °C

With lithium hydroxide; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; triethylamine; trifluoroacetic acid; In tetrahydrofuran; methanol; dichloromethane; benzene;
DOI:10.1002/chem.200601446

Reference yield:

: C₁₁H₁₃SNO₃

: 941714-78-9
C₂₁H₂₈S₂N₂O₅

Guidance literature:: Multi-step reaction with 2 steps

1: 1.64 g / benzene / 4 h / Heating

2: 92 percent / BOP-Cl; Et₃N / CH₂Cl₂ / 20 °C

With bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; triethylamine; In dichloromethane; benzene;
DOI:10.1002/chem.200601446