2-nitrosoimino-2,3-dihydro-3-(3-phenyl-5-pyrazolyl)-5-benzoyl-1,3,4-thiadiazole

Base Information

Chemical Name:2-nitrosoimino-2,3-dihydro-3-(3-phenyl-5-pyrazolyl)-5-benzoyl-1,3,4-thiadiazole
CAS No.:112565-03-4
Molecular Formula:C₁₈H₁₂N₆O₂S
Molecular Weight:376.398
Hs Code.:

Synonyms:2-nitrosoimino-2,3-dihydro-3-(3-phenyl-5-pyrazolyl)-5-benzoyl-1,3,4-thiadiazole

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Chemical Property of 2-nitrosoimino-2,3-dihydro-3-(3-phenyl-5-pyrazolyl)-5-benzoyl-1,3,4-thiadiazole

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Technology Process of 2-nitrosoimino-2,3-dihydro-3-(3-phenyl-5-pyrazolyl)-5-benzoyl-1,3,4-thiadiazole

There total 6 articles about 2-nitrosoimino-2,3-dihydro-3-(3-phenyl-5-pyrazolyl)-5-benzoyl-1,3,4-thiadiazole 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: 77.0%

: 112565-01-2
2-imino-2,3-dihydro-3-(3-phenyl-5-pyrazolyl)-5-benzoyl-1,3,4-thiadiazole

: 112565-03-4
2-nitrosoimino-2,3-dihydro-3-(3-phenyl-5-pyrazolyl)-5-benzoyl-1,3,4-thiadiazole

Guidance literature:: With acetic acid; sodium nitrite; In water; for 6h; refrigerator;

Reference yield:

: 5667-47-0
phenacyldimethylsulfonium bromide

: 112565-03-4
2-nitrosoimino-2,3-dihydro-3-(3-phenyl-5-pyrazolyl)-5-benzoyl-1,3,4-thiadiazole

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) NaNO₂/AcOH/conc. HCl; 2.) NaOAc/H₂O / 2.) EtOH, r.t., 3 h

2: 85 percent / ethanol / 4 h

3: NaNO₂ / acetic acid / 0.5 h

With hydrogenchloride; water; sodium acetate; acetic acid; sodium nitrite; In ethanol; acetic acid;

Reference yield:

: 98664-16-5
α-bromo-α'(3-phenyl)pyrazolylglyoxalhydrazone

: 112565-03-4
2-nitrosoimino-2,3-dihydro-3-(3-phenyl-5-pyrazolyl)-5-benzoyl-1,3,4-thiadiazole

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / ethanol / 4 h

2: NaNO₂ / acetic acid / 0.5 h

With sodium nitrite; In ethanol; acetic acid;