2-bromo-2-(2-tert-butoxycarbonylamino-4-pyridyl)-1-(4-fluorophenyl) ethanone

Base Information

Chemical Name:2-bromo-2-(2-tert-butoxycarbonylamino-4-pyridyl)-1-(4-fluorophenyl) ethanone
CAS No.:917813-40-2
Molecular Formula:C₁₈H₁₈BrFN₂O₃
Molecular Weight:409.255
Hs Code.:

Synonyms:2-bromo-2-(2-tert-butoxycarbonylamino-4-pyridyl)-1-(4-fluorophenyl) ethanone

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Chemical Property of 2-bromo-2-(2-tert-butoxycarbonylamino-4-pyridyl)-1-(4-fluorophenyl) ethanone

Chemical Property:

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Technology Process of 2-bromo-2-(2-tert-butoxycarbonylamino-4-pyridyl)-1-(4-fluorophenyl) ethanone

There total 4 articles about 2-bromo-2-(2-tert-butoxycarbonylamino-4-pyridyl)-1-(4-fluorophenyl) ethanone 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: 97.0%

: 365427-98-1
tert-butyl {4-[2-(4-fluorophenyl)-2-oxoethyl]-2-pyridyl}carbamate

: 917813-40-2
2-bromo-2-(2-tert-butoxycarbonylamino-4-pyridyl)-1-(4-fluorophenyl) ethanone

Guidance literature:: With N-Bromosuccinimide; In dichloromethane; acetone;
DOI:10.1039/c9pp00010k

Reference yield:

: 721929-81-3
2-(di-tert-butyloxycarbonyl)amino-4-picoline

: 917813-40-2
2-bromo-2-(2-tert-butoxycarbonylamino-4-pyridyl)-1-(4-fluorophenyl) ethanone

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hexamethyldisilazane / tetrahydrofuran / 0 °C

2: N-Bromosuccinimide / dichloromethane; acetone

With N-Bromosuccinimide; sodium hexamethyldisilazane; In tetrahydrofuran; dichloromethane; acetone;
DOI:10.1039/c9pp00010k

Reference yield:

: 695-34-1
2-Amino-4-methylpyridine

: 917813-40-2
2-bromo-2-(2-tert-butoxycarbonylamino-4-pyridyl)-1-(4-fluorophenyl) ethanone

Guidance literature:: Multi-step reaction with 4 steps

1: tert-butyl alcohol / 30 °C

2: dmap / tetrahydrofuran

3: sodium hexamethyldisilazane / tetrahydrofuran / 0 °C

4: N-Bromosuccinimide / dichloromethane; acetone

With dmap; N-Bromosuccinimide; sodium hexamethyldisilazane; In tetrahydrofuran; dichloromethane; acetone; tert-butyl alcohol;
DOI:10.1039/c9pp00010k