ethyl 5-(4-fluorophenyl)-4,5,6,7-tetrahydro-4-oxothiazolo[5,4-c]pyridine-2-carboxylate

Base Information

Chemical Name:ethyl 5-(4-fluorophenyl)-4,5,6,7-tetrahydro-4-oxothiazolo[5,4-c]pyridine-2-carboxylate
CAS No.:1312415-16-9
Molecular Formula:C₁₅H₁₃FN₂O₃S
Molecular Weight:320.344
Hs Code.:

Synonyms:ethyl 5-(4-fluorophenyl)-4,5,6,7-tetrahydro-4-oxothiazolo[5,4-c]pyridine-2-carboxylate

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of ethyl 5-(4-fluorophenyl)-4,5,6,7-tetrahydro-4-oxothiazolo[5,4-c]pyridine-2-carboxylate

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Technology Process of ethyl 5-(4-fluorophenyl)-4,5,6,7-tetrahydro-4-oxothiazolo[5,4-c]pyridine-2-carboxylate

There total 6 articles about ethyl 5-(4-fluorophenyl)-4,5,6,7-tetrahydro-4-oxothiazolo[5,4-c]pyridine-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: 68.0%

: 16982-21-1
ethyl 2-amino-2-thioxoacetate

: 1312412-94-4
3-bromo-1-(4-fluorophenyl)piperidine-2,4-dione

: 1312415-16-9
5-(4-fluorophenyl)-4-oxo-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine-2-carboxylic acid ethyl ester

Guidance literature:: With sodium hydrogencarbonate; In ethanol; at 80 ℃; for 2h;
DOI:10.1021/jm400650w

Reference yield:

: 952489-53-1
C₁₁H₁₀FNO₂

: 1312415-16-9
5-(4-fluorophenyl)-4-oxo-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine-2-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: N-Bromosuccinimide / dichloromethane / 0.5 h / 0 °C

2: sodium hydrogencarbonate / ethanol / 2 h / 80 °C

With N-Bromosuccinimide; sodium hydrogencarbonate; In ethanol; dichloromethane;

Reference yield:

: 1312412-92-2
N-(2-ethoxycarbonylethyl)-N-(4-fluorophenyl)malonamic acid ethyl ester

: 1312415-16-9
5-(4-fluorophenyl)-4-oxo-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine-2-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: sodium ethanolate / ethanol / 16 h / 85 °C

2: water; acetic acid / 16 h / 90 °C

3: N-Bromosuccinimide / dichloromethane / 0.5 h / 0 °C

4: sodium hydrogencarbonate / ethanol / 2 h / 80 °C

With N-Bromosuccinimide; water; sodium ethanolate; sodium hydrogencarbonate; acetic acid; In ethanol; dichloromethane;