8-cyano-1,4-dihydro-1-methyl-7-p-fluorophenyl-4-oxopyrrolo<1,2-a>pyrimidine-3-carboxylic acid

Base Information

Chemical Name:8-cyano-1,4-dihydro-1-methyl-7-p-fluorophenyl-4-oxopyrrolo<1,2-a>pyrimidine-3-carboxylic acid
CAS No.:111074-65-8
Molecular Formula:C₁₆H₁₀FN₃O₃
Molecular Weight:311.272
Hs Code.:

Synonyms:8-cyano-1,4-dihydro-1-methyl-7-p-fluorophenyl-4-oxopyrrolo<1,2-a>pyrimidine-3-carboxylic acid

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Chemical Property of 8-cyano-1,4-dihydro-1-methyl-7-p-fluorophenyl-4-oxopyrrolo<1,2-a>pyrimidine-3-carboxylic acid

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Technology Process of 8-cyano-1,4-dihydro-1-methyl-7-p-fluorophenyl-4-oxopyrrolo<1,2-a>pyrimidine-3-carboxylic acid

There total 7 articles about 8-cyano-1,4-dihydro-1-methyl-7-p-fluorophenyl-4-oxopyrrolo<1,2-a>pyrimidine-3-carboxylic acid 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: 79.0%

: 111074-55-6
3-carbethoxy-8-cyano-1,4-dihydro-1-ethyl-7-p-fluorophenyl-4-oxopyrrolo<1,2-a>pyrimidine

: 111074-65-8
8-cyano-1,4-dihydro-1-methyl-7-p-fluorophenyl-4-oxopyrrolo<1,2-a>pyrimidine-3-carboxylic acid

Guidance literature:: With hydrogenchloride; at 55 ℃; for 15h;
DOI:10.1002/jhet.5570240201

Reference yield:

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

: 111074-65-8
8-cyano-1,4-dihydro-1-methyl-7-p-fluorophenyl-4-oxopyrrolo<1,2-a>pyrimidine-3-carboxylic acid

Guidance literature:: Multi-step reaction with 5 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

5: 79 percent / conc. HCl / 15 h / 55 °C

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

: 111074-65-8
8-cyano-1,4-dihydro-1-methyl-7-p-fluorophenyl-4-oxopyrrolo<1,2-a>pyrimidine-3-carboxylic acid

Guidance literature:: Multi-step reaction with 4 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

4: 79 percent / conc. HCl / 15 h / 55 °C

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