C₃₁H₃₁F₃N₄O₇S

Base Information

Chemical Name:C₃₁H₃₁F₃N₄O₇S
CAS No.:1028252-79-0
Molecular Formula:C₃₁H₃₁F₃N₄O₇S
Molecular Weight:660.671
Hs Code.:

C<sub>31</sub>H<sub>31</sub>F<sub>3</sub>N<sub>4</sub>O<sub>7</sub>S

Synonyms:C₃₁H₃₁F₃N₄O₇S

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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 C₃₁H₃₁F₃N₄O₇S

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Technology Process of C₃₁H₃₁F₃N₄O₇S

There total 9 articles about C₃₁H₃₁F₃N₄O₇S 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: 54.0%

: 1028252-78-9
C₃₆H₃₉F₃N₄O₉S

: 1028252-79-0
C₃₁H₃₁F₃N₄O₇S

Guidance literature:: C₃₆H₃₉F₃N₄O₉S; With trifluoroacetic acid; In dichloromethane; 1,2-dichloro-ethane; at 20 ℃; for 1.5h;

With triethylamine; In methanol; dichloromethane;

Reference yield:

: (1S,2R)-1-{[1-Phenyl-meth-(E)-ylidene]-amino}-2-vinyl-cyclopropanecarboxylic acid ethyl ester

: 1028252-79-0
C₃₁H₃₁F₃N₄O₇S

Guidance literature:: Multi-step reaction with 8 steps

1.1: hydrogenchloride; water / tert-butyl methyl ether; toluene / 2 h / 20 °C

1.2: 0 °C / pH 14

2.1: tert-butyl methyl ether / 20 °C / Heating / reflux

3.1: sodium hydroxide / savinase 16.0 L / water; dimethyl sulfoxide / 66.66 h / 35 - 48 °C / pH 8.5 - 9 / Resolution of racemate; sodium borate buffer; Enzymatic reaction

4.1: methanol; lithium hydroxide; water / tetrahydrofuran / 20 °C

4.3: pH 4

5.1: 1,1'-carbonyldiimidazole / tetrahydrofuran / 0.83 h / Heating / reflux

5.2: 20 h / 20 °C

6.1: trifluoroacetic acid / dichloromethane / 1.5 h / 20 °C

7.1: 4-methyl-morpholine; HATU / dichloromethane / 20 °C

8.1: trifluoroacetic acid / dichloromethane; 1,2-dichloro-ethane / 1.5 h / 20 °C

With 4-methyl-morpholine; hydrogenchloride; methanol; lithium hydroxide; sodium hydroxide; water; HATU; 1,1'-carbonyldiimidazole; trifluoroacetic acid; savinase 16.0 L; In tetrahydrofuran; dichloromethane; tert-butyl methyl ether; water; dimethyl sulfoxide; 1,2-dichloro-ethane; toluene;

Reference yield:

: 213316-49-5
(1RS,2SR)-ethyl 2-vinyl-1-(tert-butoxycarbonylamino)cyclopropanecarboxylate

: 1028252-79-0
C₃₁H₃₁F₃N₄O₇S

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium hydroxide / savinase 16.0 L / water; dimethyl sulfoxide / 66.66 h / 35 - 48 °C / pH 8.5 - 9 / Resolution of racemate; sodium borate buffer; Enzymatic reaction

2.1: methanol; lithium hydroxide; water / tetrahydrofuran / 20 °C

2.3: pH 4

3.1: 1,1'-carbonyldiimidazole / tetrahydrofuran / 0.83 h / Heating / reflux

3.2: 20 h / 20 °C

4.1: trifluoroacetic acid / dichloromethane / 1.5 h / 20 °C

5.1: 4-methyl-morpholine; HATU / dichloromethane / 20 °C

6.1: trifluoroacetic acid / dichloromethane; 1,2-dichloro-ethane / 1.5 h / 20 °C

With 4-methyl-morpholine; methanol; lithium hydroxide; sodium hydroxide; water; HATU; 1,1'-carbonyldiimidazole; trifluoroacetic acid; savinase 16.0 L; In tetrahydrofuran; dichloromethane; water; dimethyl sulfoxide; 1,2-dichloro-ethane;