methyl 5-(3-(4-fluorophenyl)-7-(1-methyl-1 H-1,2,3-triazol-4-yl)-4-oxo-3,4-dihydroquinazolin-2-yl)pentanoate

Base Information

Chemical Name:methyl 5-(3-(4-fluorophenyl)-7-(1-methyl-1 H-1,2,3-triazol-4-yl)-4-oxo-3,4-dihydroquinazolin-2-yl)pentanoate
CAS No.:1373278-29-5
Molecular Formula:C₂₃H₂₂FN₅O₃
Molecular Weight:435.458
Hs Code.:

Synonyms:methyl 5-(3-(4-fluorophenyl)-7-(1-methyl-1 H-1,2,3-triazol-4-yl)-4-oxo-3,4-dihydroquinazolin-2-yl)pentanoate

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Chemical Property of methyl 5-(3-(4-fluorophenyl)-7-(1-methyl-1 H-1,2,3-triazol-4-yl)-4-oxo-3,4-dihydroquinazolin-2-yl)pentanoate

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Technology Process of methyl 5-(3-(4-fluorophenyl)-7-(1-methyl-1 H-1,2,3-triazol-4-yl)-4-oxo-3,4-dihydroquinazolin-2-yl)pentanoate

There total 7 articles about methyl 5-(3-(4-fluorophenyl)-7-(1-methyl-1 H-1,2,3-triazol-4-yl)-4-oxo-3,4-dihydroquinazolin-2-yl)pentanoate 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: 60.0%

: 1373278-28-4
methyl 5-(7-ethynyl-3-(4-fluorophenyl)-4-oxo-3,4-dihydroquinazolin-2-yl)pentanoate

: 74-88-4
methyl iodide

: 1373278-29-5
methyl 5-(3-(4-fluorophenyl)-7-(1-methyl-1 H-1,2,3-triazol-4-yl)-4-oxo-3,4-dihydroquinazolin-2-yl)pentanoate

Guidance literature:: With copper(l) iodide; sodium azide; In acetonitrile; at 50 ℃; for 14h; Inert atmosphere;

Reference yield:

: 20776-50-5
2-amino-4-bromobenzoic acid

: 1373278-29-5
methyl 5-(3-(4-fluorophenyl)-7-(1-methyl-1 H-1,2,3-triazol-4-yl)-4-oxo-3,4-dihydroquinazolin-2-yl)pentanoate

Guidance literature:: Multi-step reaction with 6 steps

1: triethylamine / dichloromethane / 0 - 40 °C

2: acetic anhydride / 5 h / 150 °C

3: acetic acid / 1 h / 100 °C

4: triethylamine; copper(l) iodide / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / N,N-dimethyl-formamide / 0.17 h / 60 °C / microwave irradiation; Inert atmosphere

5: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.67 h / -30 °C / Inert atmosphere

6: sodium azide; copper(l) iodide / acetonitrile / 14 h / 50 °C / Inert atmosphere

With copper(l) iodide; sodium azide; tetrabutyl ammonium fluoride; acetic anhydride; acetic acid; triethylamine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 35444-44-1
methyl adipoyl chloride

: 1373278-29-5
methyl 5-(3-(4-fluorophenyl)-7-(1-methyl-1 H-1,2,3-triazol-4-yl)-4-oxo-3,4-dihydroquinazolin-2-yl)pentanoate

Guidance literature:: Multi-step reaction with 6 steps

1: triethylamine / dichloromethane / 0 - 40 °C

2: acetic anhydride / 5 h / 150 °C

3: acetic acid / 1 h / 100 °C

4: triethylamine; copper(l) iodide / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / N,N-dimethyl-formamide / 0.17 h / 60 °C / microwave irradiation; Inert atmosphere

5: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.67 h / -30 °C / Inert atmosphere

6: sodium azide; copper(l) iodide / acetonitrile / 14 h / 50 °C / Inert atmosphere

With copper(l) iodide; sodium azide; tetrabutyl ammonium fluoride; acetic anhydride; acetic acid; triethylamine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; acetonitrile;