2-(6-methyl-2-oxo-4-phenyl-1,2,3,4-tetrahydropyrimidine-5-carbonyl)hydrazinecarbothioamide

Base Information

Chemical Name:2-(6-methyl-2-oxo-4-phenyl-1,2,3,4-tetrahydropyrimidine-5-carbonyl)hydrazinecarbothioamide
CAS No.:1421320-02-6
Molecular Formula:C₁₃H₁₅N₅O₂S
Molecular Weight:305.36
Hs Code.:

Synonyms:2-(6-methyl-2-oxo-4-phenyl-1,2,3,4-tetrahydropyrimidine-5-carbonyl)hydrazinecarbothioamide

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Chemical Property of 2-(6-methyl-2-oxo-4-phenyl-1,2,3,4-tetrahydropyrimidine-5-carbonyl)hydrazinecarbothioamide

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Technology Process of 2-(6-methyl-2-oxo-4-phenyl-1,2,3,4-tetrahydropyrimidine-5-carbonyl)hydrazinecarbothioamide

There total 4 articles about 2-(6-methyl-2-oxo-4-phenyl-1,2,3,4-tetrahydropyrimidine-5-carbonyl)hydrazinecarbothioamide 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: 85.0%

: 123237-03-6,5395-36-8
ethyl 6-methyl-4-phenyl-3,4-dihydropyrimidin-2(1H)-one-5-carboxylate

: 79-19-6
thiosemicarbazide

: 1421320-02-6
2-(6-methyl-2-oxo-4-phenyl-1,2,3,4-tetrahydropyrimidine-5-carbonyl)hydrazinecarbothioamide

Guidance literature:: In acetone; Reflux;

Reference yield: 83.0%

: 333-20-0
potassium thioacyanate

: 593283-24-0
6-methyl-4-phenyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carbohydrazide

: 1421320-02-6
2-(6-methyl-2-oxo-4-phenyl-1,2,3,4-tetrahydropyrimidine-5-carbonyl)hydrazinecarbothioamide

Guidance literature:: With hydrogenchloride; In water; at 4 ℃; Reflux;
DOI:10.1007/s00044-014-1005-1

Reference yield:

: 100-52-7
benzaldehyde

: 1421320-02-6
2-(6-methyl-2-oxo-4-phenyl-1,2,3,4-tetrahydropyrimidine-5-carbonyl)hydrazinecarbothioamide

Guidance literature:: Multi-step reaction with 2 steps

1: Acidic conditions

2: acetone / Reflux

In acetone; 1: |Biginelli Pyrimidone Synthesis;