tert-butyl ((6-(4-acetyl-1,3-thiazol-2-yl)-2-isobutyl-4-(4-methylphenyl)quinolin-3-yl)methyl)carbamate

Base Information

Chemical Name:tert-butyl ((6-(4-acetyl-1,3-thiazol-2-yl)-2-isobutyl-4-(4-methylphenyl)quinolin-3-yl)methyl)carbamate
CAS No.:660450-98-6
Molecular Formula:C₃₁H₃₅N₃O₃S
Molecular Weight:529.703
Hs Code.:

Synonyms:tert-butyl ((6-(4-acetyl-1,3-thiazol-2-yl)-2-isobutyl-4-(4-methylphenyl)quinolin-3-yl)methyl)carbamate

Suppliers and Price of tert-butyl ((6-(4-acetyl-1,3-thiazol-2-yl)-2-isobutyl-4-(4-methylphenyl)quinolin-3-yl)methyl)carbamate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of tert-butyl ((6-(4-acetyl-1,3-thiazol-2-yl)-2-isobutyl-4-(4-methylphenyl)quinolin-3-yl)methyl)carbamate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of tert-butyl ((6-(4-acetyl-1,3-thiazol-2-yl)-2-isobutyl-4-(4-methylphenyl)quinolin-3-yl)methyl)carbamate

There total 5 articles about tert-butyl ((6-(4-acetyl-1,3-thiazol-2-yl)-2-isobutyl-4-(4-methylphenyl)quinolin-3-yl)methyl)carbamate 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: 95.0%

: 660450-97-5
tert-butyl ((2-isobutyl-6-(4-(methoxy(methyl)carbamoyl)-1,3-thiazol-2-yl)-4-(4-methylphenyl)quinolin-3-yl)methyl)carbamate

: 660450-98-6
tert-butyl ((6-(4-acetyl-1,3-thiazol-2-yl)-2-isobutyl-4-(4-methylphenyl)quinolin-3-yl)methyl)carbamate

Guidance literature:: With methylmagnesium bromide; In tetrahydrofuran; diethyl ether; at 0 ℃; for 1h;
DOI:10.1016/j.bmcl.2017.05.048

Reference yield:

: 660449-04-7
tert-butyl {[6-hydroxy-4-(4-methylphenyl)-2-(2-methylpropyl)quinolin-3-yl]methyl}carbamate

: 660450-98-6
tert-butyl ((6-(4-acetyl-1,3-thiazol-2-yl)-2-isobutyl-4-(4-methylphenyl)quinolin-3-yl)methyl)carbamate

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 1 h / 0 - 20 °C

2.1: bis(pinacol)diborane; potassium acetate / dimethyl sulfoxide / 0.17 h / 80 °C / Inert atmosphere

2.2: 0.25 h / 100 °C / Inert atmosphere

2.3: 17 h / Inert atmosphere; Reflux

3.1: sodium hydroxide / methanol; tetrahydrofuran / 0.25 h / 20 °C

4.1: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 2 h / 20 °C

5.1: methylmagnesium bromide / tetrahydrofuran; diethyl ether / 1 h / 0 °C

With methylmagnesium bromide; potassium acetate; sodium hydride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; bis(pinacol)diborane; sodium hydroxide; In tetrahydrofuran; methanol; diethyl ether; dimethyl sulfoxide; N,N-dimethyl-formamide; mineral oil; 2.1: |Suzuki Coupling / 2.2: |Suzuki Coupling / 2.3: |Suzuki Coupling;
DOI:10.1016/j.bmcl.2017.05.048

Reference yield:

: 660449-16-1
3-{[(tert-butoxycarbonyl)amino]methyl}-4-(4-methylphenyl)-2-(2-methylpropyl)quinolin-6-yl trifluoromethanesulfonate

: 660450-98-6
tert-butyl ((6-(4-acetyl-1,3-thiazol-2-yl)-2-isobutyl-4-(4-methylphenyl)quinolin-3-yl)methyl)carbamate

Guidance literature:: Multi-step reaction with 4 steps

1.1: bis(pinacol)diborane; potassium acetate / dimethyl sulfoxide / 0.17 h / 80 °C / Inert atmosphere

1.2: 0.25 h / 100 °C / Inert atmosphere

1.3: 17 h / Inert atmosphere; Reflux

2.1: sodium hydroxide / methanol; tetrahydrofuran / 0.25 h / 20 °C

3.1: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 2 h / 20 °C

4.1: methylmagnesium bromide / tetrahydrofuran; diethyl ether / 1 h / 0 °C

With methylmagnesium bromide; potassium acetate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; bis(pinacol)diborane; sodium hydroxide; In tetrahydrofuran; methanol; diethyl ether; dimethyl sulfoxide; N,N-dimethyl-formamide; 1.1: |Suzuki Coupling / 1.2: |Suzuki Coupling / 1.3: |Suzuki Coupling;
DOI:10.1016/j.bmcl.2017.05.048