(R)-tert-butyl (4-(4-(m-tolyl)-1H-1,2,3-triazol-1-yl)-1-(2,4,5-trifluorophenyl)butan-2-yl)carbamate

Base Information

Chemical Name:(R)-tert-butyl (4-(4-(m-tolyl)-1H-1,2,3-triazol-1-yl)-1-(2,4,5-trifluorophenyl)butan-2-yl)carbamate
CAS No.:1500076-16-3
Molecular Formula:C₂₄H₂₇F₃N₄O₂
Molecular Weight:460.499
Hs Code.:

Synonyms:(R)-tert-butyl (4-(4-(m-tolyl)-1H-1,2,3-triazol-1-yl)-1-(2,4,5-trifluorophenyl)butan-2-yl)carbamate

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Chemical Property of (R)-tert-butyl (4-(4-(m-tolyl)-1H-1,2,3-triazol-1-yl)-1-(2,4,5-trifluorophenyl)butan-2-yl)carbamate

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Technology Process of (R)-tert-butyl (4-(4-(m-tolyl)-1H-1,2,3-triazol-1-yl)-1-(2,4,5-trifluorophenyl)butan-2-yl)carbamate

There total 4 articles about (R)-tert-butyl (4-(4-(m-tolyl)-1H-1,2,3-triazol-1-yl)-1-(2,4,5-trifluorophenyl)butan-2-yl)carbamate 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: 63.0%

: 766-82-5
1-ethynyl-3-methyl-benzene

: 1500076-06-1
(R)-tert-butyl (4-azido-1-(2,4,5-trifluorophenyl)butan-2-yl)carbamate

: 1500076-16-3
(R)-tert-butyl (4-(4-(m-tolyl)-1H-1,2,3-triazol-1-yl)-1-(2,4,5-trifluorophenyl)butan-2-yl)carbamate

Guidance literature:: With copper(l) iodide; sodium L-ascorbate; In water; tert-butyl alcohol; at 80 ℃; for 3h; Inert atmosphere;
DOI:10.1002/cmdc.201300104

Reference yield:

: 1048703-14-5
(R)-tert-butyl (4-hydroxy-1-(2,4,5-trifluorophenyl)butan-2-yl)carbamate

: 1500076-16-3
(R)-tert-butyl (4-(4-(m-tolyl)-1H-1,2,3-triazol-1-yl)-1-(2,4,5-trifluorophenyl)butan-2-yl)carbamate

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / dichloromethane / 0.5 h / 20 °C

2: sodium azide / N,N-dimethyl-formamide / 18 h / 67 °C

3: sodium L-ascorbate; copper(l) iodide / tert-butyl alcohol; water / 3 h / 80 °C / Inert atmosphere

With copper(l) iodide; sodium azide; sodium L-ascorbate; triethylamine; In dichloromethane; water; N,N-dimethyl-formamide; tert-butyl alcohol;
DOI:10.1002/cmdc.201300104

Reference yield:

: 881995-73-9
3-(R)-tert-butoxycarbonylamino-4-(2,4,5-trifluorophenyl)butyric acid methyl ester

: 1500076-16-3
(R)-tert-butyl (4-(4-(m-tolyl)-1H-1,2,3-triazol-1-yl)-1-(2,4,5-trifluorophenyl)butan-2-yl)carbamate

Guidance literature:: Multi-step reaction with 4 steps

1: lithium borohydride / tetrahydrofuran / 2 h / 0 - 20 °C

2: triethylamine / dichloromethane / 0.5 h / 20 °C

3: sodium azide / N,N-dimethyl-formamide / 18 h / 67 °C

4: sodium L-ascorbate; copper(l) iodide / tert-butyl alcohol; water / 3 h / 80 °C / Inert atmosphere

With copper(l) iodide; lithium borohydride; sodium azide; sodium L-ascorbate; triethylamine; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide; tert-butyl alcohol;
DOI:10.1002/cmdc.201300104