8-Cyano-7-(4-fluoro-phenyl)-4-oxo-1-prop-2-ynyl-1,4-dihydro-pyrrolo[1,2-a]pyrimidine-3-carboxylic acid ethyl ester

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Chemical Name:8-Cyano-7-(4-fluoro-phenyl)-4-oxo-1-prop-2-ynyl-1,4-dihydro-pyrrolo[1,2-a]pyrimidine-3-carboxylic acid ethyl ester
CAS No.:111074-58-9
Molecular Formula:C₂₀H₁₄FN₃O₃
Molecular Weight:363.348
Hs Code.:

Synonyms:8-Cyano-7-(4-fluoro-phenyl)-4-oxo-1-prop-2-ynyl-1,4-dihydro-pyrrolo[1,2-a]pyrimidine-3-carboxylic acid ethyl ester

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Chemical Property of 8-Cyano-7-(4-fluoro-phenyl)-4-oxo-1-prop-2-ynyl-1,4-dihydro-pyrrolo[1,2-a]pyrimidine-3-carboxylic acid ethyl ester

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Technology Process of 8-Cyano-7-(4-fluoro-phenyl)-4-oxo-1-prop-2-ynyl-1,4-dihydro-pyrrolo[1,2-a]pyrimidine-3-carboxylic acid ethyl ester

There total 7 articles about 8-Cyano-7-(4-fluoro-phenyl)-4-oxo-1-prop-2-ynyl-1,4-dihydro-pyrrolo[1,2-a]pyrimidine-3-carboxylic acid ethyl ester 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:

: 87-13-8
diethyl 2-ethoxymethylenemalonate

: 111074-58-9
8-Cyano-7-(4-fluoro-phenyl)-4-oxo-1-prop-2-ynyl-1,4-dihydro-pyrrolo[1,2-a]pyrimidine-3-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 68 percent / ethanol / 36 h / Heating

2: 1.) sodium methoxide / 1.) DMF, room temp., 10 min; 2.) room temp., 12 h

With sodium methylate; In ethanol;
DOI:10.1002/jhet.5570240201

Reference yield:

: 451-50-3
N-(2-(4-fluorophenyl)-2-oxoethyl)acetamide

: 111074-58-9
8-Cyano-7-(4-fluoro-phenyl)-4-oxo-1-prop-2-ynyl-1,4-dihydro-pyrrolo[1,2-a]pyrimidine-3-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 76 percent / 50percent aq. NaOH / H₂O; methanol / 1.) 0 deg C, 15 min; 2.) 60-65 deg C, 35 min

2: 74 percent / ethanol / Ambient temperature; overnight

3: 74 percent / potassium t-butoxide; HCl / dimethylformamide / 18 h / Ambient temperature

4: 1.) sodium methoxide / 1.) DMF, room temp., 10 min; 2.) room temp., 12 h

With hydrogenchloride; sodium hydroxide; potassium tert-butylate; sodium methylate; In methanol; ethanol; water; N,N-dimethyl-formamide;
DOI:10.1002/jhet.5570240201

Reference yield:

: 111074-43-2
2-amino-3-cyano-4-p-fluorophenylpyrrole

: 111074-58-9
8-Cyano-7-(4-fluoro-phenyl)-4-oxo-1-prop-2-ynyl-1,4-dihydro-pyrrolo[1,2-a]pyrimidine-3-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 74 percent / ethanol / Ambient temperature; overnight

2: 74 percent / potassium t-butoxide; HCl / dimethylformamide / 18 h / Ambient temperature

3: 1.) sodium methoxide / 1.) DMF, room temp., 10 min; 2.) room temp., 12 h

With hydrogenchloride; potassium tert-butylate; sodium methylate; In ethanol; N,N-dimethyl-formamide;
DOI:10.1002/jhet.5570240201