1-(1',4-dimethyl-1-phenyl-1H,1'H-3,4'-bipyrazol-5-yl)-3-(2,3,4,5-tetrahydro-1H-benzo[d]azepin-1-yl)urea

Base Information

Chemical Name:1-(1',4-dimethyl-1-phenyl-1H,1'H-3,4'-bipyrazol-5-yl)-3-(2,3,4,5-tetrahydro-1H-benzo[d]azepin-1-yl)urea
CAS No.:1610346-30-9
Molecular Formula:C₂₅H₂₇N₇O
Molecular Weight:441.536
Hs Code.:

Synonyms:1-(1',4-dimethyl-1-phenyl-1H,1'H-3,4'-bipyrazol-5-yl)-3-(2,3,4,5-tetrahydro-1H-benzo[d]azepin-1-yl)urea

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1-(1',4-dimethyl-1-phenyl-1H,1'H-3,4'-bipyrazol-5-yl)-3-(2,3,4,5-tetrahydro-1H-benzo[d]azepin-1-yl)urea

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of 1-(1',4-dimethyl-1-phenyl-1H,1'H-3,4'-bipyrazol-5-yl)-3-(2,3,4,5-tetrahydro-1H-benzo[d]azepin-1-yl)urea

There total 5 articles about 1-(1',4-dimethyl-1-phenyl-1H,1'H-3,4'-bipyrazol-5-yl)-3-(2,3,4,5-tetrahydro-1H-benzo[d]azepin-1-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: 41.27%

: 1610346-28-5
1-(1',4-dimethyl-1-phenyl-1H,1'H-3,4'-bipyrazol-5-yl)-3-(2-oxo-2,3,4,5-tetrahydro-1H-benzo[d]azepin-1-yl)urea

: 1610346-30-9
1-(1',4-dimethyl-1-phenyl-1H,1'H-3,4'-bipyrazol-5-yl)-3-(2,3,4,5-tetrahydro-1H-benzo[d]azepin-1-yl)urea

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran; at 20 ℃;

Reference yield:

: 85290-80-8
ethyl 1-methylpyrazole-4-carboxylate

: 1610346-30-9
1-(1',4-dimethyl-1-phenyl-1H,1'H-3,4'-bipyrazol-5-yl)-3-(2,3,4,5-tetrahydro-1H-benzo[d]azepin-1-yl)urea

Guidance literature:: Multi-step reaction with 5 steps

1.1: lithium hexamethyldisilazane / tetrahydrofuran / 1.5 h / -80 °C / Inert atmosphere

1.2: -76 - 20 °C / Inert atmosphere

2.1: ethanol / Reflux

3.1: sodium hydroxide / ethyl acetate; water / 2.5 h / 20 - 33 °C

4.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 2 h / 20 °C

5.1: lithium aluminium tetrahydride / tetrahydrofuran / 20 °C

With lithium aluminium tetrahydride; N-ethyl-N,N-diisopropylamine; sodium hydroxide; lithium hexamethyldisilazane; In tetrahydrofuran; ethanol; water; ethyl acetate; N,N-dimethyl-formamide;

Reference yield:

: 1414571-72-4
2-methyl-3-(1-methyl-1H-pyrazol-4-yl)-3-oxopropanenitrile

: 1610346-30-9
1-(1',4-dimethyl-1-phenyl-1H,1'H-3,4'-bipyrazol-5-yl)-3-(2,3,4,5-tetrahydro-1H-benzo[d]azepin-1-yl)urea

Guidance literature:: Multi-step reaction with 4 steps

1: ethanol / Reflux

2: sodium hydroxide / ethyl acetate; water / 2.5 h / 20 - 33 °C

3: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 2 h / 20 °C

4: lithium aluminium tetrahydride / tetrahydrofuran / 20 °C

With lithium aluminium tetrahydride; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In tetrahydrofuran; ethanol; water; ethyl acetate; N,N-dimethyl-formamide;