C₂₇H₃₉N₅O₆S

Base Information

Chemical Name:C₂₇H₃₉N₅O₆S
CAS No.:848084-11-7
Molecular Formula:C₂₇H₃₉N₅O₆S
Molecular Weight:561.703
Hs Code.:

C<sub>27</sub>H<sub>39</sub>N<sub>5</sub>O<sub>6</sub>S

Synonyms:C₂₇H₃₉N₅O₆S

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Chemical Property of C₂₇H₃₉N₅O₆S

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Technology Process of C₂₇H₃₉N₅O₆S

There total 5 articles about C₂₇H₃₉N₅O₆S 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: 58.0%

: 848084-13-9
C₁₅H₁₇N₅O₄S

: 16899-09-5
8-hydroxylauric acid

: 848084-11-7
C₂₇H₃₉N₅O₆S

Guidance literature:: With 1-hydroxy-7-aza-benzotriazole; N-ethyl-N,N-diisopropylamine; diisopropyl-carbodiimide; In N,N-dimethyl-formamide; at 20 ℃; for 18h;

Reference yield:

: 14113-01-0
Ethyl hydrogen suberate

: 848084-11-7
C₂₇H₃₉N₅O₆S

Guidance literature:: Multi-step reaction with 5 steps

1.1: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 3 h / 20 °C

2.1: zinc(II) chloride / diethyl ether / -78 - 0 °C

2.2: 2 h / 0 - 20 °C

3.1: lithium hydroxide; water / tetrahydrofuran / 18 h / 20 °C

3.2: pH 4

4.1: sodium tetrahydroborate / ethanol / 1.67 h / 0 °C

5.1: 1-hydroxy-7-aza-benzotriazole; N-ethyl-N,N-diisopropylamine; diisopropyl-carbodiimide / N,N-dimethyl-formamide / 18 h / 20 °C

With lithium hydroxide; sodium tetrahydroborate; 1-hydroxy-7-aza-benzotriazole; oxalyl dichloride; water; N-ethyl-N,N-diisopropylamine; N,N-dimethyl-formamide; zinc(II) chloride; diisopropyl-carbodiimide; In tetrahydrofuran; diethyl ether; ethanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 14113-02-1
ethyl 8-chloro-8-oxooctanoate

: 848084-11-7
C₂₇H₃₉N₅O₆S

Guidance literature:: Multi-step reaction with 4 steps

1.1: zinc(II) chloride / diethyl ether / -78 - 0 °C

1.2: 2 h / 0 - 20 °C

2.1: lithium hydroxide; water / tetrahydrofuran / 18 h / 20 °C

2.2: pH 4

3.1: sodium tetrahydroborate / ethanol / 1.67 h / 0 °C

4.1: 1-hydroxy-7-aza-benzotriazole; N-ethyl-N,N-diisopropylamine; diisopropyl-carbodiimide / N,N-dimethyl-formamide / 18 h / 20 °C

With lithium hydroxide; sodium tetrahydroborate; 1-hydroxy-7-aza-benzotriazole; water; N-ethyl-N,N-diisopropylamine; zinc(II) chloride; diisopropyl-carbodiimide; In tetrahydrofuran; diethyl ether; ethanol; N,N-dimethyl-formamide;