[3-(1-triphenylmethyl-1H-imidazol-4-yl)prop-2-ynyl]carbamic acid tert-butyl ester

Base Information

Chemical Name:[3-(1-triphenylmethyl-1H-imidazol-4-yl)prop-2-ynyl]carbamic acid tert-butyl ester
CAS No.:269064-60-0
Molecular Formula:C₃₀H₂₉N₃O₂
Molecular Weight:463.579
Hs Code.:

Synonyms:[3-(1-triphenylmethyl-1H-imidazol-4-yl)prop-2-ynyl]carbamic acid tert-butyl ester

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Chemical Property of [3-(1-triphenylmethyl-1H-imidazol-4-yl)prop-2-ynyl]carbamic acid tert-butyl ester

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Technology Process of [3-(1-triphenylmethyl-1H-imidazol-4-yl)prop-2-ynyl]carbamic acid tert-butyl ester

There total 1 articles about [3-(1-triphenylmethyl-1H-imidazol-4-yl)prop-2-ynyl]carbamic acid tert-butyl ester 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: 85.0%

: 92136-39-5
N-tert-Butoxycarbonyl-1-amino-3-propyne

: 96797-15-8
N-trityl-4⁽⁵⁾-iodoimidazole

: 269064-60-0
[3-(1-triphenylmethyl-1H-imidazol-4-yl)prop-2-ynyl]carbamic acid tert-butyl ester

Guidance literature:: With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; diisobutylamine; In tetrahydrofuran; at 20 ℃; for 20h;
DOI:10.1021/jo991395b

Reference yield: 70.0%

: 269064-60-0
[3-(1-triphenylmethyl-1H-imidazol-4-yl)prop-2-ynyl]carbamic acid tert-butyl ester

: 269064-61-1
[3-(2-azido-1-triphenylmethyl-1H-imidazol-4-yl)prop-2-ynyl]carbamic acid tert-butyl ester

Guidance literature:: With n-butyllithium; 4-toluenesulfonyl azide; In tetrahydrofuran; hexane; at -75 ℃; for 0.166667h;
DOI:10.1021/jo991395b

Reference yield:

: 269064-60-0
[3-(1-triphenylmethyl-1H-imidazol-4-yl)prop-2-ynyl]carbamic acid tert-butyl ester

: 34649-22-4
oroidin

Guidance literature:: Multi-step reaction with 5 steps

1: 70 percent / n-BuLi; tosyl azide / tetrahydrofuran; hexane / 0.17 h / -75 °C

2: 88 percent / CF₃COOH / CH₂Cl₂ / 5 h / 20 °C

3: 69 percent / Na₂CO₃ / dimethylformamide / 6 h / 20 °C

4: 74 percent / H₂ / Lindlar catalyst / methanol / 3 h / 20 °C / 760.05 Torr

5: 56 percent / aq. HCl / methanol / 6 h / 60 °C

With hydrogenchloride; n-butyllithium; 4-toluenesulfonyl azide; hydrogen; sodium carbonate; trifluoroacetic acid; Lindlar's catalyst; In tetrahydrofuran; methanol; hexane; dichloromethane; N,N-dimethyl-formamide; 1: azidation / 2: carbamate cleavage; detritylation / 3: Condensation / 4: Hydrogenation / 5: Isomerization;
DOI:10.1021/jo991395b