C₁₇H₂₃FN₄O₅S

Base Information

Chemical Name:C₁₇H₂₃FN₄O₅S
CAS No.:1402742-23-7
Molecular Formula:C₁₇H₂₃FN₄O₅S
Molecular Weight:414.458
Hs Code.:

C<sub>17</sub>H<sub>23</sub>FN<sub>4</sub>O<sub>5</sub>S

Synonyms:C₁₇H₂₃FN₄O₅S

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Chemical Property of C₁₇H₂₃FN₄O₅S

Chemical Property:

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Technology Process of C₁₇H₂₃FN₄O₅S

There total 22 articles about C₁₇H₂₃FN₄O₅S 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: 100.0%

: 1402742-21-5
C₁₇H₂₁FN₄O₇S

: 1402742-23-7
C₁₇H₂₃FN₄O₅S

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; at 25 ℃; for 16h; under 1292.9 Torr;

Reference yield:

: 1402742-06-6
C₂₈H₃₂FNO₆S

: 1402742-23-7
C₁₇H₂₃FN₄O₅S

Guidance literature:: Multi-step reaction with 10 steps

1.1: sodium hexamethyldisilazane / tetrahydrofuran / 0.5 h / -78 - -30 °C

1.2: -78 - 25 °C

2.1: hydrogen / palladium hydrogenation catalyst / ethanol

3.1: diethoxyltriphenylphosphorane / toluene / 60 h / 45 °C

4.1: water; lithium hydroxide / tetrahydrofuran / 60 °C

4.2: 25 °C / pH 3

5.1: triethylamine; diphenyl phosphoryl azide / tetrahydrofuran / 24 h / 25 °C

5.2: 1.5 h / 80 °C

6.1: trifluoroacetic acid / 1,3-Dimethoxybenzene; chloroform / 18 h

7.1: 4 h / Reflux

7.2: 12 h / 25 °C

8.1: nitric acid; sulfuric acid / 1 h / -10 °C

8.2: 12 h / 30 °C

9.1: carbon dioxide; ammonia / water; methanol / 38 °C / Resolution of racemate

10.1: hydrogen / palladium on activated charcoal / methanol / 16 h / 25 °C / 1292.9 Torr

With carbon dioxide; sulfuric acid; diphenyl phosphoryl azide; diethoxyltriphenylphosphorane; ammonia; water; hydrogen; nitric acid; sodium hexamethyldisilazane; triethylamine; trifluoroacetic acid; lithium hydroxide; palladium on activated charcoal; In tetrahydrofuran; methanol; ethanol; chloroform; water; toluene; 1,3-Dimethoxybenzene;

Reference yield:

: 1402742-07-7
C₂₉H₃₄FNO₇S

: 1402742-23-7
C₁₇H₂₃FN₄O₅S

Guidance literature:: Multi-step reaction with 9 steps

1.1: hydrogen / palladium hydrogenation catalyst / ethanol

2.1: diethoxyltriphenylphosphorane / toluene / 60 h / 45 °C

3.1: water; lithium hydroxide / tetrahydrofuran / 60 °C

3.2: 25 °C / pH 3

4.1: triethylamine; diphenyl phosphoryl azide / tetrahydrofuran / 24 h / 25 °C

4.2: 1.5 h / 80 °C

5.1: trifluoroacetic acid / 1,3-Dimethoxybenzene; chloroform / 18 h

6.1: 4 h / Reflux

6.2: 12 h / 25 °C

7.1: nitric acid; sulfuric acid / 1 h / -10 °C

7.2: 12 h / 30 °C

8.1: carbon dioxide; ammonia / water; methanol / 38 °C / Resolution of racemate

9.1: hydrogen / palladium on activated charcoal / methanol / 16 h / 25 °C / 1292.9 Torr

With carbon dioxide; sulfuric acid; diphenyl phosphoryl azide; diethoxyltriphenylphosphorane; ammonia; water; hydrogen; nitric acid; triethylamine; trifluoroacetic acid; lithium hydroxide; palladium on activated charcoal; In tetrahydrofuran; methanol; ethanol; chloroform; water; toluene; 1,3-Dimethoxybenzene;