4-allyl-1-{[(4-phenyl-5-methyl-4H-1,2,4-triazol-3-yl)sulfanyl]acetyl} thiosemicarbazide

Base Information

Chemical Name:4-allyl-1-{[(4-phenyl-5-methyl-4H-1,2,4-triazol-3-yl)sulfanyl]acetyl} thiosemicarbazide
CAS No.:6264-22-8
Molecular Formula:C₁₅H₁₈N₆OS₂
Molecular Weight:362.48
Hs Code.:

Synonyms:4-allyl-1-{[(4-phenyl-5-methyl-4H-1,2,4-triazol-3-yl)sulfanyl]acetyl} thiosemicarbazide

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Chemical Property of 4-allyl-1-{[(4-phenyl-5-methyl-4H-1,2,4-triazol-3-yl)sulfanyl]acetyl} thiosemicarbazide

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Technology Process of 4-allyl-1-{[(4-phenyl-5-methyl-4H-1,2,4-triazol-3-yl)sulfanyl]acetyl} thiosemicarbazide

There total 4 articles about 4-allyl-1-{[(4-phenyl-5-methyl-4H-1,2,4-triazol-3-yl)sulfanyl]acetyl} thiosemicarbazide 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: 83.4%

: 62373-05-1
[(4-phenyl-5-methyl-4H-1,2,4-triazol-3-yl)sulfanyl]acetohydrazide

: 57-06-7,58391-87-0
N-allyl isothiocyanate

: 6264-22-8
4-allyl-1-{[(4-phenyl-5-methyl-4H-1,2,4-triazol-3-yl)sulfanyl]acetyl} thiosemicarbazide

Guidance literature:: at 50 ℃; for 12h;
DOI:10.3109/14756366.2011.653352

Reference yield:

: 84210-55-9
ethyl [(4-phenyl-5-methyl-4H-1,2,4-triazol-3-yl)sulfanyl]acetate

: 6264-22-8
4-allyl-1-{[(4-phenyl-5-methyl-4H-1,2,4-triazol-3-yl)sulfanyl]acetyl} thiosemicarbazide

Guidance literature:: Multi-step reaction with 2 steps

1: hydrazine hydrate / ethanol / 24 h / Cooling

2: 12 h / 50 °C

With hydrazine hydrate; In ethanol;
DOI:10.3109/14756366.2011.653352

Reference yield:

: 6232-82-2
5-methyl-4-phenyl-2,4-dihydro-3H-1,2,4-triazole-3-thione

: 6264-22-8
4-allyl-1-{[(4-phenyl-5-methyl-4H-1,2,4-triazol-3-yl)sulfanyl]acetyl} thiosemicarbazide

Guidance literature:: Multi-step reaction with 3 steps

1: sodium / ethanol / 4 h

2: hydrazine hydrate / ethanol / 24 h / Cooling

3: 12 h / 50 °C

With sodium; hydrazine hydrate; In ethanol;
DOI:10.3109/14756366.2011.653352