1H-Pyrazole-4-acetamide, 5-amino-a-(benzoylamino)-1-phenyl-

Base Information

Chemical Name:1H-Pyrazole-4-acetamide, 5-amino-a-(benzoylamino)-1-phenyl-
CAS No.:110212-03-8
Molecular Formula:C₁₈H₁₇N₅O₂
Molecular Weight:335.365
Hs Code.:

Synonyms:

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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 1H-Pyrazole-4-acetamide, 5-amino-a-(benzoylamino)-1-phenyl-

Chemical Property:

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Safty Information:

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MSDS Files:: SDS file from LookChem

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Technology Process of 1H-Pyrazole-4-acetamide, 5-amino-a-(benzoylamino)-1-phenyl-

There total 5 articles about 1H-Pyrazole-4-acetamide, 5-amino-a-(benzoylamino)-1-phenyl- 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: 13.5%

: 110212-00-5
5-benzoyl-4,5-dihydro-1-phenyl-1H-pyrazolo<3,4-d>pyrimidine-4-carbonitrile

: 110212-02-7
5-amino-α-benzamido-1-phenyl-1H-pyrazole-4-acetonitrile

: 110212-03-8
5-amino-α-benzamido-1-phenyl-1H-pyrazole-4-acetamide

Guidance literature:: With hydrogenchloride; In water; dimethyl sulfoxide; for 0.5h; Ambient temperature;

Reference yield: 2.7%

: 110212-00-5
5-benzoyl-4,5-dihydro-1-phenyl-1H-pyrazolo<3,4-d>pyrimidine-4-carbonitrile

: 110212-02-7
5-amino-α-benzamido-1-phenyl-1H-pyrazole-4-acetonitrile

: 110212-03-8
5-amino-α-benzamido-1-phenyl-1H-pyrazole-4-acetamide

: 110212-04-9
5-amino-α-benzamido-1-phenyl-1H-pyrazole-4-acetate

Guidance literature:: With hydrogenchloride; In methanol; water; for 2h; Ambient temperature;

Reference yield:

: 53645-79-7
1-phenyl-1H-pyrazolo[3,4-d]pyrimidine

: 110212-03-8
5-amino-α-benzamido-1-phenyl-1H-pyrazole-4-acetamide

Guidance literature:: Multi-step reaction with 3 steps

1: 2.) AlCl₃ / 1.) methylene dichloride, 5 min; 2.) 13 h, r.t.

2: 49.5 percent / 20percent HCl / H₂O; dimethylsulfoxide / 0.5 h / Ambient temperature

3: 34 percent / 5percent Na₂CO₃, 10percent H₂O₂ / acetone / 16 h / Ambient temperature

With hydrogenchloride; aluminium trichloride; dihydrogen peroxide; sodium carbonate; In water; dimethyl sulfoxide; acetone;