2-chloro-4-(3-chlorophenyl)-α-(5-chloro-2-thienyl)-α-(1-methyl-1H-imidazol-5-yl)quinazoline-6-methanol

Base Information

Chemical Name:2-chloro-4-(3-chlorophenyl)-α-(5-chloro-2-thienyl)-α-(1-methyl-1H-imidazol-5-yl)quinazoline-6-methanol
CAS No.:406196-70-1
Molecular Formula:C₂₃H₁₅Cl₃N₄OS
Molecular Weight:501.823
Hs Code.:

Synonyms:2-chloro-4-(3-chlorophenyl)-α-(5-chloro-2-thienyl)-α-(1-methyl-1H-imidazol-5-yl)quinazoline-6-methanol

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Chemical Property of 2-chloro-4-(3-chlorophenyl)-α-(5-chloro-2-thienyl)-α-(1-methyl-1H-imidazol-5-yl)quinazoline-6-methanol

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Technology Process of 2-chloro-4-(3-chlorophenyl)-α-(5-chloro-2-thienyl)-α-(1-methyl-1H-imidazol-5-yl)quinazoline-6-methanol

There total 8 articles about 2-chloro-4-(3-chlorophenyl)-α-(5-chloro-2-thienyl)-α-(1-methyl-1H-imidazol-5-yl)quinazoline-6-methanol 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:

: 406196-69-8
[2-chloro-4-(3-chlorophenyl)-6-quinazolinyl](5-chloro-2-thienyl)methanone

: 371764-99-7
1-methyl-2-triethylsilanyl-1H-imidazole

: 406196-70-1
2-chloro-4-(3-chlorophenyl)-α-(5-chloro-2-thienyl)-α-(1-methyl-1H-imidazol-5-yl)quinazoline-6-methanol

Guidance literature:: 1-methyl-2-triethylsilanyl-1H-imidazole; With n-butyllithium; In tetrahydrofuran; hexane; at -70 ℃; for 0.25h;

[2-chloro-4-(3-chlorophenyl)-6-quinazolinyl](5-chloro-2-thienyl)methanone; In tetrahydrofuran; hexane; at -70 - 20 ℃; for 1h;

With water; In tetrahydrofuran; hexane; Further stages.;
DOI:10.1016/j.ejmech.2006.12.007

Reference yield:

: 7283-96-7
5-Chloro-2-thiophenecarboxaldehyde

: 406196-70-1
2-chloro-4-(3-chlorophenyl)-α-(5-chloro-2-thienyl)-α-(1-methyl-1H-imidazol-5-yl)quinazoline-6-methanol

Guidance literature:: Multi-step reaction with 7 steps

1.1: n-BuLi / hexane; tetrahydrofuran / 0.25 h / -70 °C

1.2: 68 percent / tetrahydrofuran; hexane / 1 h / -70 °C

2.1: 64 percent / MnO₂ / dioxane / 15 h / Heating

3.1: 100 percent / aq. TiCl₃ / tetrahydrofuran / 3 h / 20 °C

4.1: 100 percent / Et₃N / CH₂Cl₂ / 20 °C

5.1: 83 percent / ammonium acetate / dimethylsulfoxide / 4 h / 60 °C

6.1: 88 percent / POCl₃ / 2 h / 100 °C

7.1: n-BuLi / hexane; tetrahydrofuran / 0.25 h / -70 °C

7.2: 24 percent / tetrahydrofuran; hexane / 1 h / -70 - 20 °C

With ammonium acetate; manganese(IV) oxide; n-butyllithium; titanium(III) chloride; triethylamine; trichlorophosphate; In tetrahydrofuran; 1,4-dioxane; hexane; dichloromethane; dimethyl sulfoxide;
DOI:10.1016/j.ejmech.2006.12.007

Reference yield:

: 943834-86-4
[3-(3-chlorophenyl)-1,2-benzisoxazol-5-yl](5-chloro-2-thienyl)methanone

: 406196-70-1
2-chloro-4-(3-chlorophenyl)-α-(5-chloro-2-thienyl)-α-(1-methyl-1H-imidazol-5-yl)quinazoline-6-methanol

Guidance literature:: Multi-step reaction with 5 steps

1.1: 100 percent / aq. TiCl₃ / tetrahydrofuran / 3 h / 20 °C

2.1: 100 percent / Et₃N / CH₂Cl₂ / 20 °C

3.1: 83 percent / ammonium acetate / dimethylsulfoxide / 4 h / 60 °C

4.1: 88 percent / POCl₃ / 2 h / 100 °C

5.1: n-BuLi / hexane; tetrahydrofuran / 0.25 h / -70 °C

5.2: 24 percent / tetrahydrofuran; hexane / 1 h / -70 - 20 °C

With ammonium acetate; n-butyllithium; titanium(III) chloride; triethylamine; trichlorophosphate; In tetrahydrofuran; hexane; dichloromethane; dimethyl sulfoxide;
DOI:10.1016/j.ejmech.2006.12.007