5-[(1E)-3-({2-[2,4-dichloro(methyl)-3-({[2-methyl-4-(2-pyridinylmethoxy)-8-quinolinyl]oxy}methyl)anilino]-2-oxoethyl}amino)-3-oxo-1-propenyl]-2-pyridinecarboxylic acid

Base Information

Chemical Name:5-[(1E)-3-({2-[2,4-dichloro(methyl)-3-({[2-methyl-4-(2-pyridinylmethoxy)-8-quinolinyl]oxy}methyl)anilino]-2-oxoethyl}amino)-3-oxo-1-propenyl]-2-pyridinecarboxylic acid
CAS No.:194928-64-8
Molecular Formula:C₃₅H₂₉Cl₂N₅O₆
Molecular Weight:686.551
Hs Code.:

5-[(1E)-3-({2-[2,4-dichloro(methyl)-3-({[2-methyl-4-(2-pyridinylmethoxy)-8-quinolinyl]oxy}methyl)anilino]-2-oxoethyl}amino)-3-oxo-1-propenyl]-2-pyridinecarboxylic acid

Synonyms:5-[(1E)-3-({2-[2,4-dichloro(methyl)-3-({[2-methyl-4-(2-pyridinylmethoxy)-8-quinolinyl]oxy}methyl)anilino]-2-oxoethyl}amino)-3-oxo-1-propenyl]-2-pyridinecarboxylic acid

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Chemical Property of 5-[(1E)-3-({2-[2,4-dichloro(methyl)-3-({[2-methyl-4-(2-pyridinylmethoxy)-8-quinolinyl]oxy}methyl)anilino]-2-oxoethyl}amino)-3-oxo-1-propenyl]-2-pyridinecarboxylic acid

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Technology Process of 5-[(1E)-3-({2-[2,4-dichloro(methyl)-3-({[2-methyl-4-(2-pyridinylmethoxy)-8-quinolinyl]oxy}methyl)anilino]-2-oxoethyl}amino)-3-oxo-1-propenyl]-2-pyridinecarboxylic acid

There total 8 articles about 5-[(1E)-3-({2-[2,4-dichloro(methyl)-3-({[2-methyl-4-(2-pyridinylmethoxy)-8-quinolinyl]oxy}methyl)anilino]-2-oxoethyl}amino)-3-oxo-1-propenyl]-2-pyridinecarboxylic 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: 93.7%

: 194928-63-7
5-[(1E)-3-({2-[2,4-dichloro(methyl)-3-({[2-methyl-4-(2-pyridinylmethoxy)-8-quinolinyl]oxy}methyl)anilino]-2-oxoethyl}amino)-3-oxo-1-propenyl]-2-pyridinecarboxylate

: 194928-64-8
5-[(1E)-3-({2-[2,4-dichloro(methyl)-3-({[2-methyl-4-(2-pyridinylmethoxy)-8-quinolinyl]oxy}methyl)anilino]-2-oxoethyl}amino)-3-oxo-1-propenyl]-2-pyridinecarboxylic acid

Guidance literature:: With sodium hydroxide; In ethanol; at 20 ℃;
DOI:10.1021/jm030468n

Reference yield:

: 586-98-1
2-Hydroxymethylpyridine

: 194928-64-8
5-[(1E)-3-({2-[2,4-dichloro(methyl)-3-({[2-methyl-4-(2-pyridinylmethoxy)-8-quinolinyl]oxy}methyl)anilino]-2-oxoethyl}amino)-3-oxo-1-propenyl]-2-pyridinecarboxylic acid

Guidance literature:: Multi-step reaction with 5 steps

1.1: NaH / cooling

1.2: 49.2 percent / various solvent(s) / 100 °C

2.1: NaH / dimethylformamide / 0.5 h / cooling

2.2: 772 mg / dimethylformamide / 24 h / 20 °C

3.1: 65.2 percent / hydrazine monohydrate / ethanol / 4 h / Heating

4.1: 66.2 percent / 1-hydroxybenzotriazole; 1-ethoxy-3-[3-(dimethylamino)propyl]carbodiimide*HCl / dimethylformamide / 20 °C

5.1: 93.7 percent / aq. NaOH / ethanol / 20 °C

With sodium hydroxide; 1-(3-dimethylaminopropyl)-3-ethoxycarbodiimide hydrochloride; sodium hydride; benzotriazol-1-ol; hydrazine hydrate; In ethanol; N,N-dimethyl-formamide;
DOI:10.1021/jm030468n

Reference yield:

: 28507-46-2
4-chloro-8-hydroxy-2-methylquinoline

: 194928-64-8
5-[(1E)-3-({2-[2,4-dichloro(methyl)-3-({[2-methyl-4-(2-pyridinylmethoxy)-8-quinolinyl]oxy}methyl)anilino]-2-oxoethyl}amino)-3-oxo-1-propenyl]-2-pyridinecarboxylic acid

Guidance literature:: Multi-step reaction with 5 steps

1.1: NaH / cooling

1.2: 49.2 percent / various solvent(s) / 100 °C

2.1: NaH / dimethylformamide / 0.5 h / cooling

2.2: 772 mg / dimethylformamide / 24 h / 20 °C

3.1: 65.2 percent / hydrazine monohydrate / ethanol / 4 h / Heating

4.1: 66.2 percent / 1-hydroxybenzotriazole; 1-ethoxy-3-[3-(dimethylamino)propyl]carbodiimide*HCl / dimethylformamide / 20 °C

5.1: 93.7 percent / aq. NaOH / ethanol / 20 °C

With sodium hydroxide; 1-(3-dimethylaminopropyl)-3-ethoxycarbodiimide hydrochloride; sodium hydride; benzotriazol-1-ol; hydrazine hydrate; In ethanol; N,N-dimethyl-formamide;
DOI:10.1021/jm030468n