2-(1-tert-butoxycarbonylamino-1-phenylmethyl)-5-phenyl-1,3,4-oxadiazole

Base Information

Chemical Name:2-(1-tert-butoxycarbonylamino-1-phenylmethyl)-5-phenyl-1,3,4-oxadiazole
CAS No.:1126635-53-7
Molecular Formula:C₂₀H₂₁N₃O₃
Molecular Weight:351.405
Hs Code.:

Synonyms:2-(1-tert-butoxycarbonylamino-1-phenylmethyl)-5-phenyl-1,3,4-oxadiazole

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Chemical Property of 2-(1-tert-butoxycarbonylamino-1-phenylmethyl)-5-phenyl-1,3,4-oxadiazole

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Technology Process of 2-(1-tert-butoxycarbonylamino-1-phenylmethyl)-5-phenyl-1,3,4-oxadiazole

There total 9 articles about 2-(1-tert-butoxycarbonylamino-1-phenylmethyl)-5-phenyl-1,3,4-oxadiazole 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: 96.0%

: 1126635-30-0
N-[1-phenyl-1-(5-phenyl-1,3,4-oxadiazol-2-yl)methyl]acetamide

: 24424-99-5
di-tert-butyl dicarbonate

: 1126635-53-7
2-(1-tert-butoxycarbonylamino-1-phenylmethyl)-5-phenyl-1,3,4-oxadiazole

Guidance literature:: With diethylamine; In methanol; Reflux;
DOI:10.1016/j.tet.2008.11.096

Reference yield: 92.0%

: 1227858-22-1
N-Boc-2-phenylglycine N'-(α-ethoxybenzylidene)hydrazide

: 1126635-53-7
2-(1-tert-butoxycarbonylamino-1-phenylmethyl)-5-phenyl-1,3,4-oxadiazole

Guidance literature:: With acetic acid; at 50 ℃; for 4h;
DOI:10.3987/COM-09-11882

Reference yield:

: 2900-27-8
(2S)-2-[(tert-butoxycarbonyl)amino]-2-phenylethanoic acid

: 1126635-53-7
2-(1-tert-butoxycarbonylamino-1-phenylmethyl)-5-phenyl-1,3,4-oxadiazole

Guidance literature:: Multi-step reaction with 2 steps

1: carbonyl diimidazole / CH₂Cl₂ / 0 °C

2: CBr₄; Ph₃P / CH₂Cl₂ / 0 °C

With carbon tetrabromide; triphenylphosphine; 1,1'-carbonyldiimidazole; In dichloromethane;
DOI:10.1016/j.tetlet.2006.05.051