methyl 3-{4-[N-(tert-butoxycarbonyl)carbamimidoyl]phenoxy}-2-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)oxy]propanoate

Base Information

Chemical Name:methyl 3-{4-[N-(tert-butoxycarbonyl)carbamimidoyl]phenoxy}-2-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)oxy]propanoate
CAS No.:1448674-95-0
Molecular Formula:C₂₄H₂₅N₃O₈
Molecular Weight:483.478
Hs Code.:

Synonyms:methyl 3-{4-[N-(tert-butoxycarbonyl)carbamimidoyl]phenoxy}-2-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)oxy]propanoate

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Chemical Property of methyl 3-{4-[N-(tert-butoxycarbonyl)carbamimidoyl]phenoxy}-2-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)oxy]propanoate

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Technology Process of methyl 3-{4-[N-(tert-butoxycarbonyl)carbamimidoyl]phenoxy}-2-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)oxy]propanoate

There total 3 articles about methyl 3-{4-[N-(tert-butoxycarbonyl)carbamimidoyl]phenoxy}-2-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)oxy]propanoate 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: 100.0%

: 524-38-9
N-hydroxyphthalimide

: 1448674-13-2
3-[4-(tert-butoxycarbonylamino-imino-methyl)phenoxy]-2-hydroxypropionic acid methyl ester

: 1448674-95-0
methyl 3-{4-[N-(tert-butoxycarbonyl)carbamimidoyl]phenoxy}-2-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)oxy]propanoate

Guidance literature:: With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 20 ℃; for 16h;

Reference yield:

: 1448674-12-1
3-(4-carbamimidoylphenoxy)-2-hydroxypropionic acid methyl ester

: 1448674-95-0
methyl 3-{4-[N-(tert-butoxycarbonyl)carbamimidoyl]phenoxy}-2-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)oxy]propanoate

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydrogencarbonate / tetrahydrofuran; water / 3.5 h / 20 °C

2: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 16 h / 20 °C

With di-isopropyl azodicarboxylate; sodium hydrogencarbonate; triphenylphosphine; In tetrahydrofuran; water;

Reference yield:

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

: 1448674-95-0
methyl 3-{4-[N-(tert-butoxycarbonyl)carbamimidoyl]phenoxy}-2-[(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)oxy]propanoate

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydrogencarbonate / tetrahydrofuran; water / 3.5 h / 20 °C

2: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 16 h / 20 °C

With di-isopropyl azodicarboxylate; sodium hydrogencarbonate; triphenylphosphine; In tetrahydrofuran; water;