C₃₅H₄₄F₂N₆O₇S

Base Information

Chemical Name:C₃₅H₄₄F₂N₆O₇S
CAS No.:1620013-07-1
Molecular Formula:C₃₅H₄₄F₂N₆O₇S
Molecular Weight:730.833
Hs Code.:

C<sub>35</sub>H<sub>44</sub>F<sub>2</sub>N<sub>6</sub>O<sub>7</sub>S

Synonyms:C₃₅H₄₄F₂N₆O₇S

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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 C₃₅H₄₄F₂N₆O₇S

Chemical Property:

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Technology Process of C₃₅H₄₄F₂N₆O₇S

There total 23 articles about C₃₅H₄₄F₂N₆O₇S 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:

: 1620013-05-9
3-({[5-[(tert-butoxycarbonyl)amino]-2-(2,6-difluoro-3-methoxyphenyl)-1,3-thiazol-4-yl]carbonyl}amino)-4-{(3S,5R)-3-[(tert-butoxycarbonyl)amino]-5-methylpiperidin-1-yl}-6,7-dihydro-5H-cyclopenta[b]pyridin-7-yl acetate

: 1620013-07-1
C₃₅H₄₄F₂N₆O₇S

Guidance literature:: With water; sodium hydroxide; In tetrahydrofuran; methanol; at 20 - 30 ℃; for 0.333333h;

Reference yield:

: 74936-93-9
(S)-5-oxopyrrolidine-2-carbonyl chloride

: 1620013-07-1
C₃₅H₄₄F₂N₆O₇S

Guidance literature:: Multi-step reaction with 12 steps

1.1: dmap; triethylamine / ethyl acetate / 2 h / 20 - 30 °C

2.1: lithium hexamethyldisilazane / tetrahydrofuran / 1 h / -78 °C

2.2: 16 h / -78 - 30 °C

3.1: sodium tetrahydroborate / ethanol; tetrahydrofuran / 16 h / -10 - 30 °C

4.1: triethylamine / dichloromethane / 1 h / 0 °C

5.1: 18 h / 70 °C

6.1: hydrogen; palladium 10% on activated carbon / methanol / 15 h / 20 - 30 °C / 760.05 Torr

7.1: triethylamine / isopropyl alcohol / 0.67 h / 100 °C

8.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 1 h / 0 - 30 °C

9.1: 0.5 h / 90 °C / Sealed tube

10.1: iron; acetic acid / 3 h / 20 - 30 °C

11.1: N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / 3 h / 20 - 30 °C

12.1: water; sodium hydroxide / tetrahydrofuran; methanol / 0.33 h / 20 - 30 °C

With dmap; sodium tetrahydroborate; palladium 10% on activated carbon; water; hydrogen; iron; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; sodium hydroxide; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; ethanol; dichloromethane; ethyl acetate; isopropyl alcohol;

Reference yield:

: 1203651-05-1
(2S,4R)-methanesulfonic acid 2-tert-butoxycarbonylamino-5-methanesulfonyloxy-4-methyl-pentyl ester

: 1620013-07-1
C₃₅H₄₄F₂N₆O₇S

Guidance literature:: Multi-step reaction with 8 steps

1: 18 h / 70 °C

2: hydrogen; palladium 10% on activated carbon / methanol / 15 h / 20 - 30 °C / 760.05 Torr

3: triethylamine / isopropyl alcohol / 0.67 h / 100 °C

4: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 1 h / 0 - 30 °C

5: 0.5 h / 90 °C / Sealed tube

6: iron; acetic acid / 3 h / 20 - 30 °C

7: N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / 3 h / 20 - 30 °C

8: water; sodium hydroxide / tetrahydrofuran; methanol / 0.33 h / 20 - 30 °C

With palladium 10% on activated carbon; water; hydrogen; iron; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; sodium hydroxide; In tetrahydrofuran; methanol; dichloromethane; isopropyl alcohol;