C₆₁H₉₈N₆O₁₆

Base Information

Chemical Name:C₆₁H₉₈N₆O₁₆
CAS No.:1350817-22-9
Molecular Formula:C₆₁H₉₈N₆O₁₆
Molecular Weight:1171.48
Hs Code.:

C<sub>61</sub>H<sub>98</sub>N<sub>6</sub>O<sub>16</sub>

Synonyms:

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Chemical Property of C₆₁H₉₈N₆O₁₆

Chemical Property:

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Technology Process of C₆₁H₉₈N₆O₁₆

There total 13 articles about C₆₁H₉₈N₆O₁₆ 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:

: 1350817-20-7
(2S)-2-benzyloxycarbonylamino-N'-3-hydroxylpropylhexadecanamide

: 1350817-22-9
C₆₁H₉₈N₆O₁₆

Guidance literature:: Multi-step reaction with 3 steps

1: sulfur trioxide pyridine complex; triethylamine / dichloromethane; dimethyl sulfoxide / 2 h / 20 °C

2: acetic acid / dichloromethane / 0.5 h / 20 °C

3: sodium tris(acetoxy)borohydride / 1.5 h / 20 °C

With sulfur trioxide pyridine complex; sodium tris(acetoxy)borohydride; acetic acid; triethylamine; In dichloromethane; dimethyl sulfoxide;
DOI:10.1021/jm200906r

Reference yield:

: 1350817-21-8
C₂₈H₄₆N₂O₄

: 1350817-22-9
C₆₁H₉₈N₆O₁₆

Guidance literature:: Multi-step reaction with 2 steps

1: acetic acid / dichloromethane / 0.5 h / 20 °C

2: sodium tris(acetoxy)borohydride / 1.5 h / 20 °C

With sodium tris(acetoxy)borohydride; acetic acid; In dichloromethane;
DOI:10.1021/jm200906r

Reference yield:

: 1350817-18-3
(2S)-2-tert-butoxycarbonylamino-N'-3-hydroxylpropylpent-4-enamide

: 1350817-22-9
C₆₁H₉₈N₆O₁₆

Guidance literature:: Multi-step reaction with 7 steps

1: tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride / dichloromethane / 92 h / 40 °C

2: palladium 10% on activated carbon; hydrogen / methanol / 24 h / 20 °C

3: hydrogenchloride / ethyl acetate / 3 h / 20 °C

4: sodium hydrogencarbonate / water; ethyl acetate / 8 h / 0 °C

5: sulfur trioxide pyridine complex; triethylamine / dichloromethane; dimethyl sulfoxide / 2 h / 20 °C

6: acetic acid / dichloromethane / 0.5 h / 20 °C

7: sodium tris(acetoxy)borohydride / 1.5 h / 20 °C

With tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; hydrogenchloride; palladium 10% on activated carbon; hydrogen; sulfur trioxide pyridine complex; sodium tris(acetoxy)borohydride; sodium hydrogencarbonate; acetic acid; triethylamine; In methanol; dichloromethane; water; dimethyl sulfoxide; ethyl acetate;
DOI:10.1021/jm200906r