(S)-ethyl 4-(4-nitrophenyl)-6-oxo-1-tosyl-1,2,3,6-tetrahydropyridine-2-carboxylate

Base Information

Chemical Name:(S)-ethyl 4-(4-nitrophenyl)-6-oxo-1-tosyl-1,2,3,6-tetrahydropyridine-2-carboxylate
CAS No.:1528764-88-6
Molecular Formula:C₂₁H₂₀N₂O₇S
Molecular Weight:444.465
Hs Code.:

Synonyms:(S)-ethyl 4-(4-nitrophenyl)-6-oxo-1-tosyl-1,2,3,6-tetrahydropyridine-2-carboxylate

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

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Chemical Property of (S)-ethyl 4-(4-nitrophenyl)-6-oxo-1-tosyl-1,2,3,6-tetrahydropyridine-2-carboxylate

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Technology Process of (S)-ethyl 4-(4-nitrophenyl)-6-oxo-1-tosyl-1,2,3,6-tetrahydropyridine-2-carboxylate

There total 1 articles about (S)-ethyl 4-(4-nitrophenyl)-6-oxo-1-tosyl-1,2,3,6-tetrahydropyridine-2-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: 87.0%

: 80854-62-2
3-(4-nitrophenyl)but-2-enoyl chloride

: 83670-53-5
ethyl (N-tosylimino)acetate

: 1528764-88-6
(S)-ethyl 4-(4-nitrophenyl)-6-oxo-1-tosyl-1,2,3,6-tetrahydropyridine-2-carboxylate

Guidance literature:: With o-(trimethylsilyl)quinidine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; diethyl ether; at -40 ℃; enantioselective reaction; Schlenk technique; Molecular sieve; Inert atmosphere;
DOI:10.1039/c4ob00114a

Reference yield:

: 1528764-88-6
(S)-ethyl 4-(4-nitrophenyl)-6-oxo-1-tosyl-1,2,3,6-tetrahydropyridine-2-carboxylate

: 1581700-02-8
(2S,4S)-ethyl 4-(4-aminophenyl)-6-oxo-1-tosylpiperidine-2-carboxylate

: 1581700-16-4
(2R,4S)-ethyl 4-(4-aminophenyl)-6-oxo-1-tosylpiperidine-2-carboxylate

Guidance literature:: With hydrogen; palladium; In ethyl acetate; at 20 ℃; under 760.051 Torr; Overall yield = 90 %; Overall yield = 37 mg; diastereoselective reaction;
DOI:10.1039/c4ob00114a