C₃₅H₄₁FN₆O₅S

Base Information

Chemical Name:C₃₅H₄₁FN₆O₅S
CAS No.:1383575-47-0
Molecular Formula:C₃₅H₄₁FN₆O₅S
Molecular Weight:676.812
Hs Code.:

C<sub>35</sub>H<sub>41</sub>FN<sub>6</sub>O<sub>5</sub>S

Synonyms:C₃₅H₄₁FN₆O₅S

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Chemical Property of C₃₅H₄₁FN₆O₅S

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Technology Process of C₃₅H₄₁FN₆O₅S

There total 11 articles about C₃₅H₄₁FN₆O₅S 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:

: 1383575-20-9
3-Bromomethyl-5-fluoro-1-(toluene-4-sulfonyl)-1H-indole

: 1383575-42-5
tert-butyl 9-(4,6-dimethylpyrimidin-2-yl)-5-oxo-1,4,9-triazaspiro[5.5]undecane-1-carboxylate

: 1383575-47-0
C₃₅H₄₁FN₆O₅S

Guidance literature:: tert-butyl 9-(4,6-dimethylpyrimidin-2-yl)-5-oxo-1,4,9-triazaspiro[5.5]undecane-1-carboxylate; With tetra-(n-butyl)ammonium iodide; sodium hydride; In tetrahydrofuran; at 0 ℃; for 0.25h;

3-Bromomethyl-5-fluoro-1-(toluene-4-sulfonyl)-1H-indole; In tetrahydrofuran; at 0 - 20 ℃; for 0.5h;

Reference yield:

: 57611-57-1
methyl 4-amino-1-benzylpiperidine-4-carboxylate

: 1383575-47-0
C₃₅H₄₁FN₆O₅S

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium acetate; acetic acid; sodium tris(acetoxy)borohydride / dichloromethane / 0.67 h / Inert atmosphere

1.2: 0.08 h / 0 °C

2.1: trifluoroacetic acid / dichloromethane / 1.5 h / 20 °C / Inert atmosphere

2.2: 22 h / 0 °C / Reflux

3.1: N-ethyl-N,N-diisopropylamine / 1,2-dichloro-ethane / 112 h / 20 °C

4.1: hydrogen / 10 wt% Pd(OH)2 on carbon / tetrahydrofuran; methanol / 20 °C / 37503.8 Torr

5.1: N-ethyl-N,N-diisopropylamine / ethanol / 1 h / 120 °C / microwave irradiation; sealed tube

6.1: sodium hydride / tetra-(n-butyl)ammonium iodide / tetrahydrofuran / 0.25 h / 0 °C

6.2: 0.5 h / 0 - 20 °C

With hydrogen; sodium acetate; sodium tris(acetoxy)borohydride; sodium hydride; acetic acid; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; 10 wt% Pd(OH)2 on carbon; tetra-(n-butyl)ammonium iodide; In tetrahydrofuran; methanol; ethanol; dichloromethane; 1,2-dichloro-ethane;

Reference yield:

: 217489-00-4
5-fluoro-1-(p-tolylsulfonyl)indole-3-carboxaldehyde

: 1383575-47-0
C₃₅H₄₁FN₆O₅S

Guidance literature:: Multi-step reaction with 3 steps

1.1: tetrahydrofuran / 0.58 h / -10 - 0 °C

2.1: bromine / dichloromethane / 3.25 h / 0 - 20 °C / Inert atmosphere

3.1: sodium hydride / tetra-(n-butyl)ammonium iodide / tetrahydrofuran / 0.25 h / 0 °C

3.2: 0.5 h / 0 - 20 °C

With bromine; sodium hydride; tetra-(n-butyl)ammonium iodide; In tetrahydrofuran; dichloromethane;