N-{4-[(3-fluorobenzyloxy)]-chlorophenyl}-6-[2-({[2-(methanesulphonyl)ethyl]-[trifluoroacetyl]amino}methyl)-1,3-thiazol-4-yl]-(quinazolin-4-yl)-amine

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Chemical Name:N-{4-[(3-fluorobenzyloxy)]-chlorophenyl}-6-[2-({[2-(methanesulphonyl)ethyl]-[trifluoroacetyl]amino}methyl)-1,3-thiazol-4-yl]-(quinazolin-4-yl)-amine
CAS No.:443883-07-6
Molecular Formula:C₃₀H₂₄ClF₄N₅O₄S₂
Molecular Weight:694.13
Hs Code.:

Synonyms:N-{4-[(3-fluorobenzyloxy)]-chlorophenyl}-6-[2-({[2-(methanesulphonyl)ethyl]-[trifluoroacetyl]amino}methyl)-1,3-thiazol-4-yl]-(quinazolin-4-yl)-amine

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Chemical Property of N-{4-[(3-fluorobenzyloxy)]-chlorophenyl}-6-[2-({[2-(methanesulphonyl)ethyl]-[trifluoroacetyl]amino}methyl)-1,3-thiazol-4-yl]-(quinazolin-4-yl)-amine

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Technology Process of N-{4-[(3-fluorobenzyloxy)]-chlorophenyl}-6-[2-({[2-(methanesulphonyl)ethyl]-[trifluoroacetyl]amino}methyl)-1,3-thiazol-4-yl]-(quinazolin-4-yl)-amine

There total 12 articles about N-{4-[(3-fluorobenzyloxy)]-chlorophenyl}-6-[2-({[2-(methanesulphonyl)ethyl]-[trifluoroacetyl]amino}methyl)-1,3-thiazol-4-yl]-(quinazolin-4-yl)-amine 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:

: 98556-31-1
4-chloro-6-iodoquinazoline

: 443883-07-6
N-{4-[(3-fluorobenzyloxy)]-chlorophenyl}-6-[2-({[2-(methanesulphonyl)ethyl]-[trifluoroacetyl]amino}methyl)-1,3-thiazol-4-yl]-(quinazolin-4-yl)-amine

Guidance literature:: Multi-step reaction with 4 steps

1: propan-2-ol

2: Pd(PPh₃)2Cl₂

3: NBS / CH₂Cl₂

4: dimethylformamide / 70 °C

With bis-triphenylphosphine-palladium(II) chloride; N-Bromosuccinimide; In dichloromethane; N,N-dimethyl-formamide; isopropyl alcohol; 4: Hantzsch reaction;
DOI:10.1016/S0960-894X(02)01047-8

Reference yield:

: 231278-74-3
N-(trifluoroacetyl)-N-(methanesulphonylethyl)-aminomethylthioamide

: 443883-09-8
N-(4-(3-fluorobenzyloxy)-3-chlorophenyl)-(6-(2-bromoethanone)-quinazolin-4-yl)-amine

: 443883-07-6
N-{4-[(3-fluorobenzyloxy)]-chlorophenyl}-6-[2-({[2-(methanesulphonyl)ethyl]-[trifluoroacetyl]amino}methyl)-1,3-thiazol-4-yl]-(quinazolin-4-yl)-amine

Guidance literature:: In N,N-dimethyl-formamide; at 70 ℃;
DOI:10.1016/S0960-894X(02)01047-8

Reference yield:

: 231278-20-9
N-(3-chloro-4-(3-fluorobenzyloxy)phenyl)-6-iodoquinazolin-4-amine

: 443883-07-6
N-{4-[(3-fluorobenzyloxy)]-chlorophenyl}-6-[2-({[2-(methanesulphonyl)ethyl]-[trifluoroacetyl]amino}methyl)-1,3-thiazol-4-yl]-(quinazolin-4-yl)-amine

Guidance literature:: Multi-step reaction with 3 steps

1: Pd(PPh₃)2Cl₂

2: NBS / CH₂Cl₂

3: dimethylformamide / 70 °C

With bis-triphenylphosphine-palladium(II) chloride; N-Bromosuccinimide; In dichloromethane; N,N-dimethyl-formamide; 3: Hantzsch reaction;
DOI:10.1016/S0960-894X(02)01047-8