C₂₉H₃₁F₉N₆O₃

Base Information

Chemical Name:C₂₉H₃₁F₉N₆O₃
CAS No.:874502-26-8
Molecular Formula:C₂₉H₃₁F₉N₆O₃
Molecular Weight:682.589
Hs Code.:

C<sub>29</sub>H<sub>31</sub>F<sub>9</sub>N<sub>6</sub>O<sub>3</sub>

Synonyms:

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Chemical Property of C₂₉H₃₁F₉N₆O₃

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Technology Process of C₂₉H₃₁F₉N₆O₃

There total 8 articles about C₂₉H₃₁F₉N₆O₃ 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:

: (3R)-[3-(4-trifluoromethylphenylamino)pentanoyl]carbamic acid benzyl ester

: 874502-26-8
C₂₉H₃₁F₉N₆O₃

Guidance literature:: Multi-step reaction with 7 steps

1: sodium tetrahydroborate; magnesium chloride / ethanol; water

2: pyridine / 0 - 20 °C

3: palladium 10% on activated carbon; hydrogen / ethyl acetate / 760.05 Torr

4: sodium tris(acetoxy)borohydride; acetic acid / 1,1-dichloroethane / 20 °C

5: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 20 °C

6: sodium azide; triethylamine / toluene / 110 °C

7: triphenylphosphine

With pyridine; sodium tetrahydroborate; sodium azide; sodium tris(acetoxy)borohydride; palladium 10% on activated carbon; hydrogen; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; triphenylphosphine; magnesium chloride; In tetrahydrofuran; 1,1-dichloroethane; ethanol; water; ethyl acetate; toluene; 7: Mitsunobu reaction;
DOI:10.1016/j.bmcl.2012.04.042

Reference yield:

: 667937-05-5
(3R)-3-(4-trifluoromethylphenylamino)pentanoic acid amide

: 874502-26-8
C₂₉H₃₁F₉N₆O₃

Guidance literature:: Multi-step reaction with 8 steps

1: lithium tert-butoxide / tetrahydrofuran; diethyl ether / -10 - 0 °C

2: sodium tetrahydroborate; magnesium chloride / ethanol; water

3: pyridine / 0 - 20 °C

4: palladium 10% on activated carbon; hydrogen / ethyl acetate / 760.05 Torr

5: sodium tris(acetoxy)borohydride; acetic acid / 1,1-dichloroethane / 20 °C

6: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 20 °C

7: sodium azide; triethylamine / toluene / 110 °C

8: triphenylphosphine

With pyridine; sodium tetrahydroborate; sodium azide; sodium tris(acetoxy)borohydride; palladium 10% on activated carbon; hydrogen; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; triphenylphosphine; magnesium chloride; lithium tert-butoxide; In tetrahydrofuran; diethyl ether; 1,1-dichloroethane; ethanol; water; ethyl acetate; toluene; 8: Mitsunobu reaction;
DOI:10.1016/j.bmcl.2012.04.042

Reference yield:

: 261947-66-4
[2R,4S]4-amino-2-ethyl-6-trifluoromethyl-3,4-dihydro-2H-quinoline-1-carboxylic acid isopropyl ester

: 874502-26-8
C₂₉H₃₁F₉N₆O₃

Guidance literature:: Multi-step reaction with 4 steps

1: sodium tris(acetoxy)borohydride; acetic acid / 1,1-dichloroethane / 20 °C

2: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 20 °C

3: sodium azide; triethylamine / toluene / 110 °C

4: triphenylphosphine

With sodium azide; sodium tris(acetoxy)borohydride; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; triphenylphosphine; In tetrahydrofuran; 1,1-dichloroethane; toluene; 4: Mitsunobu reaction;
DOI:10.1016/j.bmcl.2012.04.042