(S)-1-(4-(1-(2-hydroxy-2-(3-(tetrahydro-2H-pyran-4-yloxy)phenyl)butyl)-1H-1,2,3-triazol-5-yl)butyl)pyrimidine-2,4(1H,3H)-dione

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Chemical Name:(S)-1-(4-(1-(2-hydroxy-2-(3-(tetrahydro-2H-pyran-4-yloxy)phenyl)butyl)-1H-1,2,3-triazol-5-yl)butyl)pyrimidine-2,4(1H,3H)-dione
CAS No.:1213254-54-6
Molecular Formula:C₂₅H₃₃N₅O₅
Molecular Weight:483.568
Hs Code.:

Synonyms:(S)-1-(4-(1-(2-hydroxy-2-(3-(tetrahydro-2H-pyran-4-yloxy)phenyl)butyl)-1H-1,2,3-triazol-5-yl)butyl)pyrimidine-2,4(1H,3H)-dione

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Chemical Property of (S)-1-(4-(1-(2-hydroxy-2-(3-(tetrahydro-2H-pyran-4-yloxy)phenyl)butyl)-1H-1,2,3-triazol-5-yl)butyl)pyrimidine-2,4(1H,3H)-dione

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Technology Process of (S)-1-(4-(1-(2-hydroxy-2-(3-(tetrahydro-2H-pyran-4-yloxy)phenyl)butyl)-1H-1,2,3-triazol-5-yl)butyl)pyrimidine-2,4(1H,3H)-dione

There total 12 articles about (S)-1-(4-(1-(2-hydroxy-2-(3-(tetrahydro-2H-pyran-4-yloxy)phenyl)butyl)-1H-1,2,3-triazol-5-yl)butyl)pyrimidine-2,4(1H,3H)-dione 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: 77.0%

: 1213255-73-2
1-(hex-5-ynyl)pyrimidine-2,4(1H,3H)-dione

: 1213256-32-6
(S)-1-azido-2-(3-(tetrahydro-2H-pyran-4-yloxy)phenyl)butan-2-ol

: 1213254-54-6
(S)-1-(4-(1-(2-hydroxy-2-(3-(tetrahydro-2H-pyran-4-yloxy)phenyl)butyl)-1H-1,2,3-triazol-5-yl)butyl)pyrimidine-2,4(1H,3H)-dione

Guidance literature:: With chloro(1,5-cyclooctadiene)(pentamethylcyclopentadiene)ruthenium(II); In 1,4-dioxane; at 80 ℃;
DOI:10.1021/jm3004174

Reference yield:

: C₁₇H₁₆N₂O₃

: 1213254-54-6
(S)-1-(4-(1-(2-hydroxy-2-(3-(tetrahydro-2H-pyran-4-yloxy)phenyl)butyl)-1H-1,2,3-triazol-5-yl)butyl)pyrimidine-2,4(1H,3H)-dione

Guidance literature:: Multi-step reaction with 2 steps

1: methylamine / methanol / 1 h / 20 °C

2: chloro(1,5-cyclooctadiene)(pentamethylcyclopentadiene)ruthenium(II) / 1,4-dioxane / 80 °C

With chloro(1,5-cyclooctadiene)(pentamethylcyclopentadiene)ruthenium(II); methylamine; In 1,4-dioxane; methanol;
DOI:10.1021/jm3004174

Reference yield:

: 616196-26-0
N-methoxy-3-(methoxymethoxy)-N-methylbenzamide

: 1213254-54-6
(S)-1-(4-(1-(2-hydroxy-2-(3-(tetrahydro-2H-pyran-4-yloxy)phenyl)butyl)-1H-1,2,3-triazol-5-yl)butyl)pyrimidine-2,4(1H,3H)-dione

Guidance literature:: Multi-step reaction with 9 steps

1.1: tetrahydrofuran; diethyl ether / 3.16 h / 0 - 20 °C

2.1: Methyltriphenylphosphonium bromide; sodium hexamethyldisilazane / tetrahydrofuran / 2 h / 0 - 20 °C

2.2: 12 h / 0 - 20 °C

3.1: AD-mix-α / water; tert-butyl alcohol / 3 h / 0 °C

4.1: triethylamine / dichloromethane / 2 h / 20 °C

5.1: acetic acid; trifluoroacetic acid / water / 3 h / 50 °C

6.1: di-isopropyl azodicarboxylate; triphenylphosphine / ethanol; toluene / 20 °C

7.1: sodium hydroxide / methanol; water / 50 °C

8.1: methanesulfonyl chloride; triethylamine / dichloromethane / 20 °C

8.2: 90 °C

9.1: chloro(1,5-cyclooctadiene)(pentamethylcyclopentadiene)ruthenium(II) / 1,4-dioxane / 80 °C

With chloro(1,5-cyclooctadiene)(pentamethylcyclopentadiene)ruthenium(II); di-isopropyl azodicarboxylate; AD-mix-α; Methyltriphenylphosphonium bromide; sodium hexamethyldisilazane; acetic acid; methanesulfonyl chloride; triethylamine; triphenylphosphine; trifluoroacetic acid; sodium hydroxide; In tetrahydrofuran; 1,4-dioxane; methanol; diethyl ether; ethanol; dichloromethane; water; toluene; tert-butyl alcohol; 2.2: Wittig reaction / 6.1: Mitsunobu reaction;
DOI:10.1021/jm3004174