methyl 4-(2-(4-fluoro-3-nitrophenyl)thiazol-4-yl)-1H-pyrrole-2-carboxylate

Base Information

Chemical Name:methyl 4-(2-(4-fluoro-3-nitrophenyl)thiazol-4-yl)-1H-pyrrole-2-carboxylate
CAS No.:1415820-47-1
Molecular Formula:C₁₅H₁₀FN₃O₄S
Molecular Weight:347.327
Hs Code.:

Synonyms:methyl 4-(2-(4-fluoro-3-nitrophenyl)thiazol-4-yl)-1H-pyrrole-2-carboxylate

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Chemical Property of methyl 4-(2-(4-fluoro-3-nitrophenyl)thiazol-4-yl)-1H-pyrrole-2-carboxylate

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Technology Process of methyl 4-(2-(4-fluoro-3-nitrophenyl)thiazol-4-yl)-1H-pyrrole-2-carboxylate

There total 5 articles about methyl 4-(2-(4-fluoro-3-nitrophenyl)thiazol-4-yl)-1H-pyrrole-2-carboxylate 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: 70.3%

: 1415820-00-6
methyl 4-(2-chloroacetyl)-1H-pyrrole-2-carboxylate

: 1415820-46-0
4-fluoro-3-nitrobenzothioamide

: 1415820-47-1
methyl 4-(2-(4-fluoro-3-nitrophenyl)thiazol-4-yl)-1H-pyrrole-2-carboxylate

Guidance literature:: With acetic acid; for 2h; Reflux;

Reference yield:

: 400-94-2
4-fluoro-3-nitrobenzoyl chloride

: 1415820-47-1
methyl 4-(2-(4-fluoro-3-nitrophenyl)thiazol-4-yl)-1H-pyrrole-2-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: ammonia / toluene; methanol / 0.25 h / 20 °C

2.1: Lawessons reagent / 1,2-dimethoxyethane; tetrahydrofuran / 2 h / 50 °C

2.2: 1 h / 20 °C

3.1: acetic acid / 2 h / Reflux

With Lawessons reagent; ammonia; acetic acid; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; toluene;

Reference yield:

: 1193-62-0
methyl Pyrrole-2-carboxylate

: 1415820-47-1
methyl 4-(2-(4-fluoro-3-nitrophenyl)thiazol-4-yl)-1H-pyrrole-2-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: aluminum (III) chloride / dichloromethane / Reflux

2: acetic acid / 2 h / Reflux

With aluminum (III) chloride; acetic acid; In dichloromethane;