2-Hydroxy-N-(1-methyl-1-{1-methyl-1-[1-methyl-1-(methyl-phenyl-carbamoyl)-ethylcarbamoyl]-ethylcarbamoyl}-ethyl)-benzamide

Base Information

Chemical Name:2-Hydroxy-N-(1-methyl-1-{1-methyl-1-[1-methyl-1-(methyl-phenyl-carbamoyl)-ethylcarbamoyl]-ethylcarbamoyl}-ethyl)-benzamide
CAS No.:192046-69-8
Molecular Formula:C₂₆H₃₄N₄O₅
Molecular Weight:482.58
Hs Code.:

Synonyms:2-Hydroxy-N-(1-methyl-1-{1-methyl-1-[1-methyl-1-(methyl-phenyl-carbamoyl)-ethylcarbamoyl]-ethylcarbamoyl}-ethyl)-benzamide

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Chemical Property of 2-Hydroxy-N-(1-methyl-1-{1-methyl-1-[1-methyl-1-(methyl-phenyl-carbamoyl)-ethylcarbamoyl]-ethylcarbamoyl}-ethyl)-benzamide

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Technology Process of 2-Hydroxy-N-(1-methyl-1-{1-methyl-1-[1-methyl-1-(methyl-phenyl-carbamoyl)-ethylcarbamoyl]-ethylcarbamoyl}-ethyl)-benzamide

There total 4 articles about 2-Hydroxy-N-(1-methyl-1-{1-methyl-1-[1-methyl-1-(methyl-phenyl-carbamoyl)-ethylcarbamoyl]-ethylcarbamoyl}-ethyl)-benzamide 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%

: 75755-40-7
2,2-dimethyl-3-(N-methyl-N-phenylamino)-2H-azirine

: 192046-66-5
2-[2-(2-Hydroxy-benzoylamino)-2-methyl-propionylamino]-2-methyl-propionic acid

: 192046-69-8
2-Hydroxy-N-(1-methyl-1-{1-methyl-1-[1-methyl-1-(methyl-phenyl-carbamoyl)-ethylcarbamoyl]-ethylcarbamoyl}-ethyl)-benzamide

Guidance literature:: In acetonitrile; Ambient temperature;
DOI:10.1002/hlca.19970800312

Reference yield:

: 69-72-7,25496-36-0,8052-31-1
salicylic acid

: 192046-69-8
2-Hydroxy-N-(1-methyl-1-{1-methyl-1-[1-methyl-1-(methyl-phenyl-carbamoyl)-ethylcarbamoyl]-ethylcarbamoyl}-ethyl)-benzamide

Guidance literature:: Multi-step reaction with 5 steps

1: 99 percent / acetonitrile / 0 deg C, then room temp., overnight

2: 6N HCl / tetrahydrofuran / 0 deg C, then room temp., overnight

3: 91 percent / acetonitrile / 0 deg C, then -> room temp., overnight

4: 3N HCl / tetrahydrofuran; H₂O / 0 deg C, then room temp., overnight

5: 89 percent / acetonitrile / Ambient temperature

With hydrogenchloride; In tetrahydrofuran; water; acetonitrile;
DOI:10.1002/hlca.19970800312

Reference yield:

: 192046-36-9
2-hydroxy-N-[1-methyl-1-(N-methyl-N-phenylcarbamoyl)ethyl]benzamide

: 192046-69-8
2-Hydroxy-N-(1-methyl-1-{1-methyl-1-[1-methyl-1-(methyl-phenyl-carbamoyl)-ethylcarbamoyl]-ethylcarbamoyl}-ethyl)-benzamide

Guidance literature:: Multi-step reaction with 4 steps

1: 6N HCl / tetrahydrofuran / 0 deg C, then room temp., overnight

2: 91 percent / acetonitrile / 0 deg C, then -> room temp., overnight

3: 3N HCl / tetrahydrofuran; H₂O / 0 deg C, then room temp., overnight

4: 89 percent / acetonitrile / Ambient temperature

With hydrogenchloride; In tetrahydrofuran; water; acetonitrile;
DOI:10.1002/hlca.19970800312