methyl 2-<3-<3--N-(4-methylpentyl)carbamoylmethyl>ureido>phenyl>acetate

Base Information

Chemical Name:methyl 2-<3-<3--N-(4-methylpentyl)carbamoylmethyl>ureido>phenyl>acetate
CAS No.:237748-29-7
Molecular Formula:C₃₃H₄₀N₄O₆
Molecular Weight:588.704
Hs Code.:

methyl 2-<3-<3-<N-<2-(N-methyl-N-phenylcarbamoylmethoxy)phenyl>-N-(4-methylpentyl)carbamoylmethyl>ureido>phenyl>acetate

Synonyms:methyl 2-<3-<3--N-(4-methylpentyl)carbamoylmethyl>ureido>phenyl>acetate

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Chemical Property of methyl 2-<3-<3--N-(4-methylpentyl)carbamoylmethyl>ureido>phenyl>acetate

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Technology Process of methyl 2-<3-<3--N-(4-methylpentyl)carbamoylmethyl>ureido>phenyl>acetate

There total 9 articles about methyl 2-<3-<3--N-(4-methylpentyl)carbamoylmethyl>ureido>phenyl>acetate 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: 82.0%

: 237748-25-3
methyl 2-<3-<3--N-(4-methyl-3-pentenyl)carbamoylmethyl>ureido>phenyl>acetate

: 237748-29-7
methyl 2-<3-<3--N-(4-methylpentyl)carbamoylmethyl>ureido>phenyl>acetate

Guidance literature:: With hydrogen; palladium on activated charcoal; In tetrahydrofuran; methanol; for 3h; under 760 Torr;
DOI:10.1248/cpb.47.755

Reference yield:

: 2270-59-9
1-bromo-4-methylpent-3-ene

: 237748-29-7
methyl 2-<3-<3--N-(4-methylpentyl)carbamoylmethyl>ureido>phenyl>acetate

Guidance literature:: Multi-step reaction with 5 steps

1: 56 percent / K₂CO₃ / dimethylformamide / 48 h / 70 °C

2: pyridine / CH₂Cl₂ / 1 h / Ambient temperature

3: hydrazine monohydrate / ethanol; CHCl₃ / Ambient temperature

4: 1.) THF, RT, 10 min, 2.) toluene, reflux, 1 h

5: 82 percent / H₂ / 5 percent Pd/C / methanol; tetrahydrofuran / 3 h / 760 Torr

With pyridine; hydrogen; potassium carbonate; hydrazine hydrate; palladium on activated charcoal; In tetrahydrofuran; methanol; ethanol; dichloromethane; chloroform; N,N-dimethyl-formamide;
DOI:10.1248/cpb.47.755

Reference yield:

: 1878-87-1
2-nitrophenoxyacetic acid

: 237748-29-7
methyl 2-<3-<3--N-(4-methylpentyl)carbamoylmethyl>ureido>phenyl>acetate

Guidance literature:: Multi-step reaction with 7 steps

1: 94 percent / EDC*HCl, DMAP / CH₂Cl₂ / 72 h / Ambient temperature

2: 91 percent / H₂ / 5 percent Pd/C / methanol / 2.5 h / 760 Torr

3: 56 percent / K₂CO₃ / dimethylformamide / 48 h / 70 °C

4: pyridine / CH₂Cl₂ / 1 h / Ambient temperature

5: hydrazine monohydrate / ethanol; CHCl₃ / Ambient temperature

6: 1.) THF, RT, 10 min, 2.) toluene, reflux, 1 h

7: 82 percent / H₂ / 5 percent Pd/C / methanol; tetrahydrofuran / 3 h / 760 Torr

With pyridine; dmap; hydrogen; potassium carbonate; hydrazine hydrate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; palladium on activated charcoal; In tetrahydrofuran; methanol; ethanol; dichloromethane; chloroform; N,N-dimethyl-formamide;
DOI:10.1248/cpb.47.755