(R)-2-(N-(2-(4-(16-fluoro-2,5,8,11,14-pentaoxahexadecyl)-1H-1,2,3-triazol-1-yl)ethyl)-4-(2-fluoroethoxy)phenylsulfonamido)-N-hydroxy-3-methylbutanamide

Base Information

Chemical Name:(R)-2-(N-(2-(4-(16-fluoro-2,5,8,11,14-pentaoxahexadecyl)-1H-1,2,3-triazol-1-yl)ethyl)-4-(2-fluoroethoxy)phenylsulfonamido)-N-hydroxy-3-methylbutanamide
CAS No.:1449846-57-4
Molecular Formula:C₂₈H₄₅F₂N₅O₁₀S
Molecular Weight:681.756
Hs Code.:

(R)-2-(N-(2-(4-(16-fluoro-2,5,8,11,14-pentaoxahexadecyl)-1H-1,2,3-triazol-1-yl)ethyl)-4-(2-fluoroethoxy)phenylsulfonamido)-N-hydroxy-3-methylbutanamide

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Chemical Property of (R)-2-(N-(2-(4-(16-fluoro-2,5,8,11,14-pentaoxahexadecyl)-1H-1,2,3-triazol-1-yl)ethyl)-4-(2-fluoroethoxy)phenylsulfonamido)-N-hydroxy-3-methylbutanamide

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Technology Process of (R)-2-(N-(2-(4-(16-fluoro-2,5,8,11,14-pentaoxahexadecyl)-1H-1,2,3-triazol-1-yl)ethyl)-4-(2-fluoroethoxy)phenylsulfonamido)-N-hydroxy-3-methylbutanamide

There total 5 articles about (R)-2-(N-(2-(4-(16-fluoro-2,5,8,11,14-pentaoxahexadecyl)-1H-1,2,3-triazol-1-yl)ethyl)-4-(2-fluoroethoxy)phenylsulfonamido)-N-hydroxy-3-methylbutanamide 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: 40.0%

: 1378928-87-0
1-fluoro-3,6,9,12,15-pentaoxaoctadec-17-yne

: 1449846-47-2
(R)-2-(N-(2-azidoethyl)-4-(2-fluoroethoxy)phenylsulfonamido)-N-hydroxy-3-methylbutanamide

: 1449846-57-4
(R)-2-(N-(2-(4-(16-fluoro-2,5,8,11,14-pentaoxahexadecyl)-1H-1,2,3-triazol-1-yl)ethyl)-4-(2-fluoroethoxy)phenylsulfonamido)-N-hydroxy-3-methylbutanamide

Guidance literature:: With copper(ll) sulfate pentahydrate; sodium L-ascorbate; In water; N,N-dimethyl-formamide; at 20 ℃; for 4h;
DOI:10.1021/jm4006753

Reference yield:

: tert-butyl (R)-2-(4-(2-fluoroethoxy)phenylsulfonamido)-3-methylbutanoate

: 1449846-57-4
(R)-2-(N-(2-(4-(16-fluoro-2,5,8,11,14-pentaoxahexadecyl)-1H-1,2,3-triazol-1-yl)ethyl)-4-(2-fluoroethoxy)phenylsulfonamido)-N-hydroxy-3-methylbutanamide

Guidance literature:: Multi-step reaction with 5 steps

1: potassium carbonate / N,N-dimethyl-formamide / 48 h / 50 °C

2: montmorillonite KSF clay / acetonitrile / 3 h / Reflux

3: 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 16 h / 20 °C

4: hydrogenchloride / 1,4-dioxane; methanol / 1.5 h / 20 °C

5: copper(ll) sulfate pentahydrate; sodium L-ascorbate / water; N,N-dimethyl-formamide / 4 h / 20 °C

With 4-methyl-morpholine; hydrogenchloride; copper(ll) sulfate pentahydrate; potassium carbonate; benzotriazol-1-ol; sodium L-ascorbate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In 1,4-dioxane; methanol; water; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/jm4006753

Reference yield:

: 1449846-35-8
(R)-tert-butyl 2-(N-(2-azidoethyl)-4-(2-fluoroethoxy)phenylsulfonamido)-3-methylbutanoate

: 1449846-57-4
(R)-2-(N-(2-(4-(16-fluoro-2,5,8,11,14-pentaoxahexadecyl)-1H-1,2,3-triazol-1-yl)ethyl)-4-(2-fluoroethoxy)phenylsulfonamido)-N-hydroxy-3-methylbutanamide

Guidance literature:: Multi-step reaction with 4 steps

1: montmorillonite KSF clay / acetonitrile / 3 h / Reflux

2: 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 16 h / 20 °C

3: hydrogenchloride / 1,4-dioxane; methanol / 1.5 h / 20 °C

4: copper(ll) sulfate pentahydrate; sodium L-ascorbate / water; N,N-dimethyl-formamide / 4 h / 20 °C

With 4-methyl-morpholine; hydrogenchloride; copper(ll) sulfate pentahydrate; benzotriazol-1-ol; sodium L-ascorbate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In 1,4-dioxane; methanol; water; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/jm4006753