Methyl 4-[((1S)-1-(4-fluorophenyl)-2-{methyl[(4-nitrophenyl)sulfonyl]amino}ethyl)amino]-2-methylquinazoline-8-carboxylate

Base Information

Chemical Name:Methyl 4-[((1S)-1-(4-fluorophenyl)-2-{methyl[(4-nitrophenyl)sulfonyl]amino}ethyl)amino]-2-methylquinazoline-8-carboxylate
CAS No.:1357080-52-4
Molecular Formula:C₂₆H₂₄FN₅O₆S
Molecular Weight:553.571
Hs Code.:

Synonyms:Methyl 4-[((1S)-1-(4-fluorophenyl)-2-{methyl[(4-nitrophenyl)sulfonyl]amino}ethyl)amino]-2-methylquinazoline-8-carboxylate

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Chemical Property of Methyl 4-[((1S)-1-(4-fluorophenyl)-2-{methyl[(4-nitrophenyl)sulfonyl]amino}ethyl)amino]-2-methylquinazoline-8-carboxylate

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Technology Process of Methyl 4-[((1S)-1-(4-fluorophenyl)-2-{methyl[(4-nitrophenyl)sulfonyl]amino}ethyl)amino]-2-methylquinazoline-8-carboxylate

There total 5 articles about Methyl 4-[((1S)-1-(4-fluorophenyl)-2-{methyl[(4-nitrophenyl)sulfonyl]amino}ethyl)amino]-2-methylquinazoline-8-carboxylate 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:

: 39622-79-2
2-aminoisophthalic acid

: 1357080-52-4
Methyl 4-[((1S)-1-(4-fluorophenyl)-2-{methyl[(4-nitrophenyl)sulfonyl]amino}ethyl)amino]-2-methylquinazoline-8-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1.1: 4 h / 140 °C

2.1: ammonium hydroxide; ammonium acetate / 2 h / 80 °C

3.1: sulfuric acid / Reflux

3.2: pH 6 - 7

4.1: N-ethyl-N,N-diisopropylamine; trichlorophosphate; N-benzyl-N,N,N-triethylammonium chloride / acetonitrile / 0.5 h / 90 °C

5.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 72 h / 70 °C

With ammonium hydroxide; sulfuric acid; ammonium acetate; N-benzyl-N,N,N-triethylammonium chloride; N-ethyl-N,N-diisopropylamine; trichlorophosphate; In acetonitrile;

Reference yield:

: 1357073-35-8
methyl 4-chloro-2-methylquinazoline-8-carboxylate

: 1357079-93-6
N-[(2S)-2-amino-2-(4-fluorophenyl)ethyl]-N-methyl-4-nitrobenzenesulfonamide

: 1357080-52-4
Methyl 4-[((1S)-1-(4-fluorophenyl)-2-{methyl[(4-nitrophenyl)sulfonyl]amino}ethyl)amino]-2-methylquinazoline-8-carboxylate

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In acetonitrile; at 70 ℃; for 72h;

Reference yield:

: 1357079-85-6
methyl 2-methyl-4-oxo-3,4-dihydroquinazoline-8-carboxylate

: 1357080-52-4
Methyl 4-[((1S)-1-(4-fluorophenyl)-2-{methyl[(4-nitrophenyl)sulfonyl]amino}ethyl)amino]-2-methylquinazoline-8-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: N-ethyl-N,N-diisopropylamine; trichlorophosphate; N-benzyl-N,N,N-triethylammonium chloride / acetonitrile / 0.5 h / 90 °C

2: N-ethyl-N,N-diisopropylamine / acetonitrile / 72 h / 70 °C

With N-benzyl-N,N,N-triethylammonium chloride; N-ethyl-N,N-diisopropylamine; trichlorophosphate; In acetonitrile;