C₂₃H₃₅N₇O₇S

Base Information

Chemical Name:C₂₃H₃₅N₇O₇S
CAS No.:201355-26-2
Molecular Formula:C₂₃H₃₅N₇O₇S
Molecular Weight:553.64
Hs Code.:

C<sub>23</sub>H<sub>35</sub>N<sub>7</sub>O<sub>7</sub>S

Synonyms:C₂₃H₃₅N₇O₇S

Suppliers and Price of C₂₃H₃₅N₇O₇S

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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 C₂₃H₃₅N₇O₇S

Chemical Property:

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Technology Process of C₂₃H₃₅N₇O₇S

There total 15 articles about C₂₃H₃₅N₇O₇S 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:

: 21568-87-6
2-aminocaprolactam

: 201355-26-2
C₂₃H₃₅N₇O₇S

Guidance literature:: Multi-step reaction with 6 steps

1: 99 percent / NaHCO₃ / tetrahydrofuran / 0 - 20 °C

2: 1.) LiHMDS / 1.) THF, RT, 2.) THF, from 0 deg C to RT

3: 100 percent / HCl / ethyl acetate / 0 - 20 °C

4: Et₃N / acetonitrile / 0 - 20 °C

5: 95 percent / aq. LiOH / ethanol / 0 - 20 °C

6: EDC, HOBt, DIPEA / acetonitrile

With hydrogenchloride; lithium hydroxide; sodium hydrogencarbonate; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; N-ethyl-N,N-diisopropylamine; lithium hexamethyldisilazane; In tetrahydrofuran; ethanol; ethyl acetate; acetonitrile;
DOI:10.1021/jm960572n

Reference yield:

: 76944-95-1
tert-butyl N-[(3S)-2-oxoazepan-3-yl]carbamate

: 201355-26-2
C₂₃H₃₅N₇O₇S

Guidance literature:: Multi-step reaction with 5 steps

1: 1.) LiHMDS / 1.) THF, RT, 2.) THF, from 0 deg C to RT

2: 100 percent / HCl / ethyl acetate / 0 - 20 °C

3: Et₃N / acetonitrile / 0 - 20 °C

4: 95 percent / aq. LiOH / ethanol / 0 - 20 °C

5: EDC, HOBt, DIPEA / acetonitrile

With hydrogenchloride; lithium hydroxide; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; N-ethyl-N,N-diisopropylamine; lithium hexamethyldisilazane; In ethanol; ethyl acetate; acetonitrile;
DOI:10.1021/jm960572n

Reference yield:

: 1939-99-7
benzenesulfonyl chloride

: 201355-26-2
C₂₃H₃₅N₇O₇S

Guidance literature:: Multi-step reaction with 3 steps

1: Et₃N / acetonitrile / 0 - 20 °C

2: 95 percent / aq. LiOH / ethanol / 0 - 20 °C

3: EDC, HOBt, DIPEA / acetonitrile

With lithium hydroxide; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; N-ethyl-N,N-diisopropylamine; In ethanol; acetonitrile;
DOI:10.1021/jm960572n