[(2-{(3R,4S)-4-[2-(Bis-carboxymethyl-amino)-phenoxy]-tetrahydro-furan-3-yloxy}-4-methyl-phenyl)-carboxymethyl-amino]-acetic acid

Base Information

Chemical Name:[(2-{(3R,4S)-4-[2-(Bis-carboxymethyl-amino)-phenoxy]-tetrahydro-furan-3-yloxy}-4-methyl-phenyl)-carboxymethyl-amino]-acetic acid
CAS No.:114158-03-1
Molecular Formula:C₂₅H₂₈N₂O₁₁
Molecular Weight:532.504
Hs Code.:

Synonyms:[(2-{(3R,4S)-4-[2-(Bis-carboxymethyl-amino)-phenoxy]-tetrahydro-furan-3-yloxy}-4-methyl-phenyl)-carboxymethyl-amino]-acetic acid

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Chemical Property of [(2-{(3R,4S)-4-[2-(Bis-carboxymethyl-amino)-phenoxy]-tetrahydro-furan-3-yloxy}-4-methyl-phenyl)-carboxymethyl-amino]-acetic acid

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Technology Process of [(2-{(3R,4S)-4-[2-(Bis-carboxymethyl-amino)-phenoxy]-tetrahydro-furan-3-yloxy}-4-methyl-phenyl)-carboxymethyl-amino]-acetic acid

There total 5 articles about [(2-{(3R,4S)-4-[2-(Bis-carboxymethyl-amino)-phenoxy]-tetrahydro-furan-3-yloxy}-4-methyl-phenyl)-carboxymethyl-amino]-acetic 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:

: 446-34-4
2-fluoro-4-methyl-1-nitrobenzene

: 114158-03-1
[(2-{(3R,4S)-4-[2-(Bis-carboxymethyl-amino)-phenoxy]-tetrahydro-furan-3-yloxy}-4-methyl-phenyl)-carboxymethyl-amino]-acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 63 percent / 57percent NaH / 1,2-dimethoxy-ethane / 1 h / Ambient temperature

2: H₂ / 5percent Pd/C / ethyl acetate; aq. ethanol / 2 h / Ambient temperature

3: 1.) 1,8-bis(dimethylamino)naphthalene, NaI; 2.) 1M KOH then acid / 1.) CH₃CN, reflux, 16 h.; 2.) dioxane, methanol, water

With potassium hydroxide; hydrogen; N,N,N',N'-tetramethyl-1,8-diaminonaphthalene; sodium hydride; sodium iodide; palladium on activated charcoal; In 1,2-dimethoxyethane; ethanol; ethyl acetate;
DOI:10.1021/ja00218a034

Reference yield:

: 114157-78-7
cis-3-(2-nitrophenoxy)tetrahydrofuran-4-ol

: 114158-03-1
[(2-{(3R,4S)-4-[2-(Bis-carboxymethyl-amino)-phenoxy]-tetrahydro-furan-3-yloxy}-4-methyl-phenyl)-carboxymethyl-amino]-acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 63 percent / 57percent NaH / 1,2-dimethoxy-ethane / 1 h / Ambient temperature

2: H₂ / 5percent Pd/C / ethyl acetate; aq. ethanol / 2 h / Ambient temperature

3: 1.) 1,8-bis(dimethylamino)naphthalene, NaI; 2.) 1M KOH then acid / 1.) CH₃CN, reflux, 16 h.; 2.) dioxane, methanol, water

With potassium hydroxide; hydrogen; N,N,N',N'-tetramethyl-1,8-diaminonaphthalene; sodium hydride; sodium iodide; palladium on activated charcoal; In 1,2-dimethoxyethane; ethanol; ethyl acetate;
DOI:10.1021/ja00218a034

Reference yield:

: 114157-85-6
(3R,4S)-3-(5-Methyl-2-nitro-phenoxy)-4-(2-nitro-phenoxy)-tetrahydro-furan

: 114158-03-1
[(2-{(3R,4S)-4-[2-(Bis-carboxymethyl-amino)-phenoxy]-tetrahydro-furan-3-yloxy}-4-methyl-phenyl)-carboxymethyl-amino]-acetic acid

Guidance literature:: Multi-step reaction with 2 steps

1: H₂ / 5percent Pd/C / ethyl acetate; aq. ethanol / 2 h / Ambient temperature

2: 1.) 1,8-bis(dimethylamino)naphthalene, NaI; 2.) 1M KOH then acid / 1.) CH₃CN, reflux, 16 h.; 2.) dioxane, methanol, water

With potassium hydroxide; hydrogen; N,N,N',N'-tetramethyl-1,8-diaminonaphthalene; sodium iodide; palladium on activated charcoal; In ethanol; ethyl acetate;
DOI:10.1021/ja00218a034