3-(1-Oxo-3-phenylamino-1,3-dihydro-isoindol-2-ylmethyl)-thiophene-2-carboxylic acid

Base Information

• Chemical Name: 3-(1-Oxo-3-phenylamino-1,3-dihydro-isoindol-2-ylmethyl)-thiophene-2-carboxylic acid
• CAS No.: 203264-32-8
• Molecular Formula: C₂₀H₁₆N₂O₃S
• Molecular Weight: 364.425
• Mol file: 203264-32-8.mol

Synonyms:3-(1-Oxo-3-phenylamino-1,3-dihydro-isoindol-2-ylmethyl)-thiophene-2-carboxylic acid

Chemical Property of 3-(1-Oxo-3-phenylamino-1,3-dihydro-isoindol-2-ylmethyl)-thiophene-2-carboxylic acid

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 3-(1-Oxo-3-phenylamino-1,3-dihydro-isoindol-2-ylmethyl)-thiophene-2-carboxylic acid

There total 3 articles about 3-(1-Oxo-3-phenylamino-1,3-dihydro-isoindol-2-ylmethyl)-thiophene-2-carboxylic 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: 89.0%

3-(1-Oxo-3-phenylamino-1,3-dihydro-isoindol-2-ylmethyl)-thiophene-2-carboxylic acid methyl ester (203264-28-2) → 3-(1-Oxo-3-phenylamino-1,3-dihydro-isoindol-2-ylmethyl)-thiophene-2-carboxylic acid (203264-32-8)

Guidance literature:

With water; potassium carbonate; In methanol; for 2h; Heating;

DOI:10.1016/S0040-4020(97)10359-3

Reference yield:

3-(1,3-Dioxo-1,3-dihydro-isoindol-2-ylmethyl)-thiophene-2-carboxylic acid methyl ester (191273-50-4) → 3-(1-Oxo-3-phenylamino-1,3-dihydro-isoindol-2-ylmethyl)-thiophene-2-carboxylic acid (203264-32-8)

Guidance literature:

Multi-step reaction with 3 steps

1: 94 percent / NaBH₄, conc. HCl / methanol; ethanol / 0.5 h / 10 - 20 °C

2: 1.) SOCl₂, 2.) Et₃N / 1) CH₂Cl₂, 30 min; 2) CH₂Cl₂, 5 min; 3) CH₂Cl₂, 1 h

3: 89 percent / potassium carbonate, water / methanol / 2 h / Heating

With hydrogenchloride; sodium tetrahydroborate; thionyl chloride; water; potassium carbonate; triethylamine; In methanol; ethanol;

DOI:10.1016/S0040-4020(97)10359-3

Reference yield:

3-(1-Hydroxy-3-oxo-1,3-dihydro-isoindol-2-ylmethyl)-thiophene-2-carboxylic acid methyl ester (203264-24-8) → 3-(1-Oxo-3-phenylamino-1,3-dihydro-isoindol-2-ylmethyl)-thiophene-2-carboxylic acid (203264-32-8)

Guidance literature:

Multi-step reaction with 2 steps

1: 1.) SOCl₂, 2.) Et₃N / 1) CH₂Cl₂, 30 min; 2) CH₂Cl₂, 5 min; 3) CH₂Cl₂, 1 h

2: 89 percent / potassium carbonate, water / methanol / 2 h / Heating

With thionyl chloride; water; potassium carbonate; triethylamine; In methanol;

DOI:10.1016/S0040-4020(97)10359-3

upstream raw materials:

3-(1-Oxo-3-phenylamino-1,3-dihydro-isoindol-2-ylmethyl)-thiophene-2-carboxylic acid methyl ester

3-(1,3-Dioxo-1,3-dihydro-isoindol-2-ylmethyl)-thiophene-2-carboxylic acid methyl ester

3-(1-Hydroxy-3-oxo-1,3-dihydro-isoindol-2-ylmethyl)-thiophene-2-carboxylic acid methyl ester