3-(4-benzyloxy-phenyl)-2-(2-tert-butoxycarbonylamino-2-ethoxycarbonyl-thioacetylamino)-propionic acid methyl ester

Base Information

Chemical Name:3-(4-benzyloxy-phenyl)-2-(2-tert-butoxycarbonylamino-2-ethoxycarbonyl-thioacetylamino)-propionic acid methyl ester
CAS No.:222976-06-9
Molecular Formula:C₂₇H₃₄N₂O₇S
Molecular Weight:530.642
Hs Code.:

3-(4-benzyloxy-phenyl)-2-(2-<i>tert</i>-butoxycarbonylamino-2-ethoxycarbonyl-thioacetylamino)-propionic acid methyl ester

Synonyms:3-(4-benzyloxy-phenyl)-2-(2-tert-butoxycarbonylamino-2-ethoxycarbonyl-thioacetylamino)-propionic acid methyl ester

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Chemical Property of 3-(4-benzyloxy-phenyl)-2-(2-tert-butoxycarbonylamino-2-ethoxycarbonyl-thioacetylamino)-propionic acid methyl ester

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Technology Process of 3-(4-benzyloxy-phenyl)-2-(2-tert-butoxycarbonylamino-2-ethoxycarbonyl-thioacetylamino)-propionic acid methyl ester

There total 5 articles about 3-(4-benzyloxy-phenyl)-2-(2-tert-butoxycarbonylamino-2-ethoxycarbonyl-thioacetylamino)-propionic acid methyl 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: 75.0%

: 222976-48-9
N-[2-(4-benzyloxy-phenyl)-1-methoxycarbonyl-ethyl]-2-tert-butoxycarbonylamino-malonamic acid ethyl ester

: 222976-06-9
3-(4-benzyloxy-phenyl)-2-(2-tert-butoxycarbonylamino-2-ethoxycarbonyl-thioacetylamino)-propionic acid methyl ester

Guidance literature:: With Lawessons reagent; In toluene; at 70 ℃; for 3h;
DOI:10.1016/S0040-4020(99)00084-8

Reference yield:

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

: 222976-06-9
3-(4-benzyloxy-phenyl)-2-(2-tert-butoxycarbonylamino-2-ethoxycarbonyl-thioacetylamino)-propionic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: KHCO₃ / H₂O; tetrahydrofuran; dioxane / 1.) 0 deg C, 2 h, 2.) room temperature

2: KOH / ethanol / 0 °C

3: 95 percent / DCC, 4-methylmorpholine / CH₂Cl₂; dimethylformamide / 0 °C

4: 75 percent / Lawesson's reagent / toluene / 3 h / 70 °C

With Lawessons reagent; 4-methyl-morpholine; potassium hydroxide; potassium hydrogencarbonate; dicyclohexyl-carbodiimide; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; water; N,N-dimethyl-formamide; toluene;
DOI:10.1016/S0040-4020(99)00084-8

Reference yield:

: 13433-00-6
diethyl aminomalonate hydrochloride

: 222976-06-9
3-(4-benzyloxy-phenyl)-2-(2-tert-butoxycarbonylamino-2-ethoxycarbonyl-thioacetylamino)-propionic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: KHCO₃ / H₂O; tetrahydrofuran; dioxane / 1.) 0 deg C, 2 h, 2.) room temperature

2: KOH / ethanol / 0 °C

3: 95 percent / DCC, 4-methylmorpholine / CH₂Cl₂; dimethylformamide / 0 °C

4: 75 percent / Lawesson's reagent / toluene / 3 h / 70 °C

With Lawessons reagent; 4-methyl-morpholine; potassium hydroxide; potassium hydrogencarbonate; dicyclohexyl-carbodiimide; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; water; N,N-dimethyl-formamide; toluene;
DOI:10.1016/S0040-4020(99)00084-8