2-({5-[(E)-3-(4-Hydroxy-3-methoxy-phenyl)-acryloylamino]-[1,3,4]thiadiazol-2-ylmethyl}-amino)-benzoic acid

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Chemical Name:2-({5-[(E)-3-(4-Hydroxy-3-methoxy-phenyl)-acryloylamino]-[1,3,4]thiadiazol-2-ylmethyl}-amino)-benzoic acid
CAS No.:497871-09-7
Molecular Formula:C₂₀H₁₈N₄O₅S
Molecular Weight:426.453
Hs Code.:

Synonyms:2-({5-[(E)-3-(4-Hydroxy-3-methoxy-phenyl)-acryloylamino]-[1,3,4]thiadiazol-2-ylmethyl}-amino)-benzoic acid

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Chemical Property of 2-({5-[(E)-3-(4-Hydroxy-3-methoxy-phenyl)-acryloylamino]-[1,3,4]thiadiazol-2-ylmethyl}-amino)-benzoic acid

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Technology Process of 2-({5-[(E)-3-(4-Hydroxy-3-methoxy-phenyl)-acryloylamino]-[1,3,4]thiadiazol-2-ylmethyl}-amino)-benzoic acid

There total 5 articles about 2-({5-[(E)-3-(4-Hydroxy-3-methoxy-phenyl)-acryloylamino]-[1,3,4]thiadiazol-2-ylmethyl}-amino)-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: 55.0%

: 121-33-5,8014-42-4
vanillin

: 497871-03-1
N-[(5'-acetylamino-1',3',4'-thiadiazol-2'-yl)methyl]anthranilic acid

: 497871-09-7
2-({5-[(E)-3-(4-Hydroxy-3-methoxy-phenyl)-acryloylamino]-[1,3,4]thiadiazol-2-ylmethyl}-amino)-benzoic acid

Guidance literature:: With sodium hydroxide; In methanol; for 10h; Heating;
DOI:10.1016/S0223-5234(02)01340-5

Reference yield:

: 65992-17-8
N-(ethoxycarbonylmethyl)anthranilic acid

: 497871-09-7
2-({5-[(E)-3-(4-Hydroxy-3-methoxy-phenyl)-acryloylamino]-[1,3,4]thiadiazol-2-ylmethyl}-amino)-benzoic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: 75 percent / methanol / 10 h / Heating

2.1: conc. H₂SO₄ / 20 °C

2.2: 62 percent / liquid ammonia / H₂O / cool

3.1: 65 percent / benzene

4.1: 55 percent / 2 percent NaOH / methanol / 10 h / Heating

With sodium hydroxide; sulfuric acid; In methanol; benzene;
DOI:10.1016/S0223-5234(02)01340-5

Reference yield:

: 118-92-3,159201-01-1,50816-84-7,80206-34-4,104809-47-4
anthranilic acid

: 497871-09-7
2-({5-[(E)-3-(4-Hydroxy-3-methoxy-phenyl)-acryloylamino]-[1,3,4]thiadiazol-2-ylmethyl}-amino)-benzoic acid

Guidance literature:: Multi-step reaction with 5 steps

1.1: 60 percent / K₂CO₃ / acetone / 15 h / Heating

2.1: 75 percent / methanol / 10 h / Heating

3.1: conc. H₂SO₄ / 20 °C

3.2: 62 percent / liquid ammonia / H₂O / cool

4.1: 65 percent / benzene

5.1: 55 percent / 2 percent NaOH / methanol / 10 h / Heating

With sodium hydroxide; sulfuric acid; potassium carbonate; In methanol; acetone; benzene;
DOI:10.1016/S0223-5234(02)01340-5