C₂₆H₂₇N₅O₅S

Base Information

Chemical Name:C₂₆H₂₇N₅O₅S
CAS No.:1027236-11-8
Molecular Formula:C₂₆H₂₇N₅O₅S
Molecular Weight:521.597
Hs Code.:

C<sub>26</sub>H<sub>27</sub>N<sub>5</sub>O<sub>5</sub>S

Synonyms:

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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 C₂₆H₂₇N₅O₅S

Chemical Property:

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Technology Process of C₂₆H₂₇N₅O₅S

There total 8 articles about C₂₆H₂₇N₅O₅S 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:

: (S)-1-((R)-2-Amino-3,3-diphenyl-propionyl)-pyrrolidine-2-carboxylic acid (5-cyano-furan-2-ylmethyl)-amide

: 1027236-11-8
C₂₆H₂₇N₅O₅S

Guidance literature:: With sulphamoyl chloride; triethylamine; In dichloromethane;
DOI:10.1021/jm030025j

Reference yield:

: 617-90-3
2-furancarbonitrile

: 1027236-11-8
C₂₆H₂₇N₅O₅S

Guidance literature:: Multi-step reaction with 8 steps

1: n-BuLi / tetrahydrofuran / -78 °C

2: NaBH₄ / methanol / 20 °C

3: CBr₄; PPh₃ / CH₂Cl₂

4: NaH / tetrahydrofuran

5: HCl / ethyl acetate

6: EDC; HOBT; Et₃N / dimethylformamide / 20 °C

7: HCl / ethyl acetate / 20 °C

8: sulfamoyl chloride; Et₃N / CH₂Cl₂

With hydrogenchloride; sodium tetrahydroborate; n-butyllithium; carbon tetrabromide; sulphamoyl chloride; sodium hydride; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; triphenylphosphine; In tetrahydrofuran; methanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/jm030025j

Reference yield:

: 42061-89-2
5-cyano-2-furancarboxaldehyde

: 1027236-11-8
C₂₆H₂₇N₅O₅S

Guidance literature:: Multi-step reaction with 7 steps

1: NaBH₄ / methanol / 20 °C

2: CBr₄; PPh₃ / CH₂Cl₂

3: NaH / tetrahydrofuran

4: HCl / ethyl acetate

5: EDC; HOBT; Et₃N / dimethylformamide / 20 °C

6: HCl / ethyl acetate / 20 °C

7: sulfamoyl chloride; Et₃N / CH₂Cl₂

With hydrogenchloride; sodium tetrahydroborate; carbon tetrabromide; sulphamoyl chloride; sodium hydride; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; triphenylphosphine; In tetrahydrofuran; methanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/jm030025j