tert-butyl 2-(2-oxo-3-(phenylmethylsulfonamido)-6-propylpyridin-1(2H)-yl)acetate

Base Information

Chemical Name:tert-butyl 2-(2-oxo-3-(phenylmethylsulfonamido)-6-propylpyridin-1(2H)-yl)acetate
CAS No.:214153-51-2
Molecular Formula:C₂₁H₂₈N₂O₅S
Molecular Weight:420.53
Hs Code.:
Mol file:214153-51-2.mol

Synonyms:tert-butyl 2-(2-oxo-3-(phenylmethylsulfonamido)-6-propylpyridin-1(2H)-yl)acetate

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Chemical Property of tert-butyl 2-(2-oxo-3-(phenylmethylsulfonamido)-6-propylpyridin-1(2H)-yl)acetate

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Technology Process of tert-butyl 2-(2-oxo-3-(phenylmethylsulfonamido)-6-propylpyridin-1(2H)-yl)acetate

There total 3 articles about tert-butyl 2-(2-oxo-3-(phenylmethylsulfonamido)-6-propylpyridin-1(2H)-yl)acetate 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:

: 187163-98-0
6-cyclopropyl-3-nitropyridin-2(1H)-one

: 214153-51-2
(2-Oxo-3-phenylmethanesulfonylamino-6-propyl-2H-pyridin-1-yl)-acetic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: NaH / tetrahydrofuran

2: H₂ / 10percent Pd/C / ethyl acetate / 760 Torr

3: pyridine

With pyridine; hydrogen; sodium hydride; palladium on activated charcoal; In tetrahydrofuran; ethyl acetate;
DOI:10.1016/S0960-894X(98)00297-2

Reference yield:

: 187163-99-1
(6-Cyclopropyl-3-nitro-2-oxo-2H-pyridin-1-yl)-acetic acid tert-butyl ester

: 214153-51-2
(2-Oxo-3-phenylmethanesulfonylamino-6-propyl-2H-pyridin-1-yl)-acetic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: H₂ / 10percent Pd/C / ethyl acetate / 760 Torr

2: pyridine

With pyridine; hydrogen; palladium on activated charcoal; In ethyl acetate;
DOI:10.1016/S0960-894X(98)00297-2