1-(4-(4-chlorophenyl)thiazol-2-yl)-3-methylindeno[1,2-c]pyrazol-4(1H)-one

Base Information

Chemical Name:1-(4-(4-chlorophenyl)thiazol-2-yl)-3-methylindeno[1,2-c]pyrazol-4(1H)-one
CAS No.:1609240-28-9
Molecular Formula:C₂₀H₁₂ClN₃OS
Molecular Weight:377.854
Hs Code.:

Synonyms:1-(4-(4-chlorophenyl)thiazol-2-yl)-3-methylindeno[1,2-c]pyrazol-4(1H)-one

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Chemical Property of 1-(4-(4-chlorophenyl)thiazol-2-yl)-3-methylindeno[1,2-c]pyrazol-4(1H)-one

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Technology Process of 1-(4-(4-chlorophenyl)thiazol-2-yl)-3-methylindeno[1,2-c]pyrazol-4(1H)-one

There total 5 articles about 1-(4-(4-chlorophenyl)thiazol-2-yl)-3-methylindeno[1,2-c]pyrazol-4(1H)-one 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: 69.0%

: 1609240-20-1
2-(1-(2-(4-(4-chlorophenyl)thiazol-2-yl)hydrazono)ethyl)-1H-indene-1,3(2H)-dione

: 1609240-28-9
1-(4-(4-chlorophenyl)thiazol-2-yl)-3-methylindeno[1,2-c]pyrazol-4(1H)-one

Guidance literature:: With acetic acid; In ethanol; for 5h; Reflux;
DOI:10.1002/jhet.1081

Reference yield:

: 1133-72-8
2-acetyl-indan-1,3-dione

: 1609240-28-9
1-(4-(4-chlorophenyl)thiazol-2-yl)-3-methylindeno[1,2-c]pyrazol-4(1H)-one

Guidance literature:: Multi-step reaction with 2 steps

1: ethanol / Reflux

2: acetic acid / ethanol / 5 h / Reflux

With acetic acid; In ethanol;
DOI:10.1002/jhet.1081

Reference yield:

: 325699-54-5
C₁₂H₁₁N₃O₂S

: 1609240-28-9
1-(4-(4-chlorophenyl)thiazol-2-yl)-3-methylindeno[1,2-c]pyrazol-4(1H)-one

Guidance literature:: Multi-step reaction with 2 steps

1: sodium acetate / ethanol / 0.5 h / Reflux

2: acetic acid / ethanol / 5 h / Reflux

With sodium acetate; acetic acid; In ethanol;
DOI:10.1002/jhet.1081