methyl 5-{3-(4-fluorophenyl)-4-oxo-7-[1-(pyridin-3-yl)-1H-1,2,3-triazol-4-yl]-3,4-dihydroquinazolin-2-yl}pentanoate

Base Information

Chemical Name:methyl 5-{3-(4-fluorophenyl)-4-oxo-7-[1-(pyridin-3-yl)-1H-1,2,3-triazol-4-yl]-3,4-dihydroquinazolin-2-yl}pentanoate
CAS No.:1373278-71-7
Molecular Formula:C₂₇H₂₃FN₆O₃
Molecular Weight:498.516
Hs Code.:

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

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

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

There total 7 articles about methyl 5-{3-(4-fluorophenyl)-4-oxo-7-[1-(pyridin-3-yl)-1H-1,2,3-triazol-4-yl]-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: 61.0%

: 1120-90-7
3-iodopyridine

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

: 1373278-71-7
methyl 5-{3-(4-fluorophenyl)-4-oxo-7-[1-(pyridin-3-yl)-1H-1,2,3-triazol-4-yl]-3,4-dihydroquinazolin-2-yl}pentanoate

Guidance literature:: With sodium azide; copper(ll) sulfate pentahydrate; sodium carbonate; sodium L-ascorbate; L-proline; In water; dimethyl sulfoxide; at 65 ℃; for 16h;

Reference yield:

: 35444-44-1
methyl adipoyl chloride

: 1373278-71-7
methyl 5-{3-(4-fluorophenyl)-4-oxo-7-[1-(pyridin-3-yl)-1H-1,2,3-triazol-4-yl]-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; L-proline; sodium carbonate; sodium L-ascorbate; copper(ll) sulfate pentahydrate / water; dimethyl sulfoxide / 16 h / 65 °C

With copper(l) iodide; sodium azide; copper(ll) sulfate pentahydrate; tetrabutyl ammonium fluoride; acetic anhydride; sodium carbonate; acetic acid; sodium L-ascorbate; triethylamine; L-proline; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; dichloromethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide;

Reference yield:

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

: 1373278-71-7
methyl 5-{3-(4-fluorophenyl)-4-oxo-7-[1-(pyridin-3-yl)-1H-1,2,3-triazol-4-yl]-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; L-proline; sodium carbonate; sodium L-ascorbate; copper(ll) sulfate pentahydrate / water; dimethyl sulfoxide / 16 h / 65 °C

With copper(l) iodide; sodium azide; copper(ll) sulfate pentahydrate; tetrabutyl ammonium fluoride; acetic anhydride; sodium carbonate; acetic acid; sodium L-ascorbate; triethylamine; L-proline; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; dichloromethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide;