2-{4-[2-(S)-allyloxycarbonylamino-2-(2-trimethylsilanylethoxycarbonyl)ethyl]phenylamino}-benzoic acid

Base Information

Chemical Name:2-{4-[2-(S)-allyloxycarbonylamino-2-(2-trimethylsilanylethoxycarbonyl)ethyl]phenylamino}-benzoic acid
CAS No.:582308-05-2
Molecular Formula:C₂₅H₃₂N₂O₆Si
Molecular Weight:484.624
Hs Code.:

Synonyms:2-{4-[2-(S)-allyloxycarbonylamino-2-(2-trimethylsilanylethoxycarbonyl)ethyl]phenylamino}-benzoic acid

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Chemical Property of 2-{4-[2-(S)-allyloxycarbonylamino-2-(2-trimethylsilanylethoxycarbonyl)ethyl]phenylamino}-benzoic acid

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Technology Process of 2-{4-[2-(S)-allyloxycarbonylamino-2-(2-trimethylsilanylethoxycarbonyl)ethyl]phenylamino}-benzoic acid

There total 5 articles about 2-{4-[2-(S)-allyloxycarbonylamino-2-(2-trimethylsilanylethoxycarbonyl)ethyl]phenylamino}-benzoic acid 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:

: 2937-50-0
Allyl chloroformate

: 2-{4-[2-amino-2-(2-trimethylsilanylethoxycarbonyl)ethyl]phenylamino}-benzoic acid hydrochloride

: 582308-05-2
2-{4-[2-(S)-allyloxycarbonylamino-2-(2-trimethylsilanylethoxycarbonyl)ethyl]phenylamino}-benzoic acid

Guidance literature:: With sodium hydrogencarbonate; In ethyl acetate; at 20 ℃; for 1h;
DOI:10.1021/jm034088d

Reference yield:

: 1488-42-2,109545-72-4
Diphenyliodonium-2-carboxylate

: 582308-05-2
2-{4-[2-(S)-allyloxycarbonylamino-2-(2-trimethylsilanylethoxycarbonyl)ethyl]phenylamino}-benzoic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 6.97 g / Cu(OAc)2 / dimethylformamide / 2 h / 100 °C

2: 6.1 g / HCl / dioxane / 1 h

3: 6.55 g / aq. NaHCO₃ / ethyl acetate / 1 h / 20 °C

With hydrogenchloride; copper diacetate; sodium hydrogencarbonate; In 1,4-dioxane; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/jm034088d

Reference yield:

: 174833-40-0
N-α-tert-butyloxycarbonyl-β-(p-aminophenyl)-L-alanine 2-(trimethylsilyl)ethyl ester

: 582308-05-2
2-{4-[2-(S)-allyloxycarbonylamino-2-(2-trimethylsilanylethoxycarbonyl)ethyl]phenylamino}-benzoic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 6.97 g / Cu(OAc)2 / dimethylformamide / 2 h / 100 °C

2: 6.1 g / HCl / dioxane / 1 h

3: 6.55 g / aq. NaHCO₃ / ethyl acetate / 1 h / 20 °C

With hydrogenchloride; copper diacetate; sodium hydrogencarbonate; In 1,4-dioxane; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/jm034088d