1-(3-acetyl-4-methyl-1-phenyl-1H-pyrazol-5-yl)-3-((3S,4R)-4-(3,4-difluorophenyl)-1-(2-methoxyethyl)pyrrolidin-3-yl)urea

Base Information

Chemical Name:1-(3-acetyl-4-methyl-1-phenyl-1H-pyrazol-5-yl)-3-((3S,4R)-4-(3,4-difluorophenyl)-1-(2-methoxyethyl)pyrrolidin-3-yl)urea
CAS No.:1610373-94-8
Molecular Formula:C₂₆H₂₉F₂N₅O₃
Molecular Weight:497.545
Hs Code.:

Synonyms:1-(3-acetyl-4-methyl-1-phenyl-1H-pyrazol-5-yl)-3-((3S,4R)-4-(3,4-difluorophenyl)-1-(2-methoxyethyl)pyrrolidin-3-yl)urea

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Chemical Property of 1-(3-acetyl-4-methyl-1-phenyl-1H-pyrazol-5-yl)-3-((3S,4R)-4-(3,4-difluorophenyl)-1-(2-methoxyethyl)pyrrolidin-3-yl)urea

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Technology Process of 1-(3-acetyl-4-methyl-1-phenyl-1H-pyrazol-5-yl)-3-((3S,4R)-4-(3,4-difluorophenyl)-1-(2-methoxyethyl)pyrrolidin-3-yl)urea

There total 6 articles about 1-(3-acetyl-4-methyl-1-phenyl-1H-pyrazol-5-yl)-3-((3S,4R)-4-(3,4-difluorophenyl)-1-(2-methoxyethyl)pyrrolidin-3-yl)urea 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: 57.0%

: 1414567-34-2
(3S,4R)-4-(3,4-difluorophenyl)-1-(2-methoxyethyl)pyrrolidin-3-amine

: 1610374-17-8
phenyl (3-acetyl-4-methyl-1-phenyl-1H-pyrazol-5-yl)carbamate

: 1610373-94-8
1-(3-acetyl-4-methyl-1-phenyl-1H-pyrazol-5-yl)-3-((3S,4R)-4-(3,4-difluorophenyl)-1-(2-methoxyethyl)pyrrolidin-3-yl)urea

Guidance literature:: In isopropyl alcohol; at 20 ℃; for 16h; Reflux;

Reference yield:

: 1367870-32-3
5-amino-4-methyl-1-phenyl-1H-pyrazole-3-carboxylic acid

: 1610373-94-8
1-(3-acetyl-4-methyl-1-phenyl-1H-pyrazol-5-yl)-3-((3S,4R)-4-(3,4-difluorophenyl)-1-(2-methoxyethyl)pyrrolidin-3-yl)urea

Guidance literature:: Multi-step reaction with 4 steps

1: HATU; N-ethyl-N,N-diisopropylamine / acetonitrile / 1.5 h / 20 °C

2: dichloromethane; diethyl ether / 3.25 h / 0 - 20 °C / Inert atmosphere

3: sodium hydroxide / ethyl acetate / 17 h / 20 °C

4: isopropyl alcohol / 16 h / 20 °C / Reflux

With N-ethyl-N,N-diisopropylamine; HATU; sodium hydroxide; In diethyl ether; dichloromethane; ethyl acetate; isopropyl alcohol; acetonitrile;

Reference yield:

: 1610374-15-6
5-amino-N-methoxy-N,4-dimethyl-1-phenyl-1H-pyrazole-3-carboxamide

: 1610373-94-8
1-(3-acetyl-4-methyl-1-phenyl-1H-pyrazol-5-yl)-3-((3S,4R)-4-(3,4-difluorophenyl)-1-(2-methoxyethyl)pyrrolidin-3-yl)urea

Guidance literature:: Multi-step reaction with 3 steps

1: dichloromethane; diethyl ether / 3.25 h / 0 - 20 °C / Inert atmosphere

2: sodium hydroxide / ethyl acetate / 17 h / 20 °C

3: isopropyl alcohol / 16 h / 20 °C / Reflux

With sodium hydroxide; In diethyl ether; dichloromethane; ethyl acetate; isopropyl alcohol;