(2S,6R)-N-(2-nitrobenzenesulfonyl)-6-pent-4-enyl-2-propyl-1,2,3,6-tetrahydropyridine

Base Information

Chemical Name:(2S,6R)-N-(2-nitrobenzenesulfonyl)-6-pent-4-enyl-2-propyl-1,2,3,6-tetrahydropyridine
CAS No.:850538-37-3
Molecular Formula:C₁₉H₂₆N₂O₄S
Molecular Weight:378.492
Hs Code.:

Synonyms:(2S,6R)-N-(2-nitrobenzenesulfonyl)-6-pent-4-enyl-2-propyl-1,2,3,6-tetrahydropyridine

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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 (2S,6R)-N-(2-nitrobenzenesulfonyl)-6-pent-4-enyl-2-propyl-1,2,3,6-tetrahydropyridine

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Technology Process of (2S,6R)-N-(2-nitrobenzenesulfonyl)-6-pent-4-enyl-2-propyl-1,2,3,6-tetrahydropyridine

There total 8 articles about (2S,6R)-N-(2-nitrobenzenesulfonyl)-6-pent-4-enyl-2-propyl-1,2,3,6-tetrahydropyridine 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: 96.0%

: 850538-39-5
N-(R)-cyclohex-2-enyl-2-nitro-N-((S)-1-propylbut-3-enyl)benzenesulfonamide

: 850538-37-3
(2S,6R)-N-(2-nitrobenzenesulfonyl)-6-pent-4-enyl-2-propyl-1,2,3,6-tetrahydropyridine

Guidance literature:: With ethene; Grubbs catalyst first generation; In dichloromethane; at 50 ℃; for 24h;
DOI:10.1021/ol0474610

Reference yield:

: 850538-40-8
(S)-2-nitro-N-(1-propylbut-3-enyl)benzenesulfonamide

: 850538-37-3
(2S,6R)-N-(2-nitrobenzenesulfonyl)-6-pent-4-enyl-2-propyl-1,2,3,6-tetrahydropyridine

Guidance literature:: Multi-step reaction with 2 steps

1: 83 percent / PPh₃; DIAD / tetrahydrofuran / 72 h / 20 °C

2: 96 percent / ethylene / Grubbs I catalyst / CH₂Cl₂ / 24 h / 50 °C

With ethene; di-isopropyl azodicarboxylate; triphenylphosphine; Grubbs catalyst first generation; In tetrahydrofuran; dichloromethane; 1: Mitsunobu reaction;
DOI:10.1021/ol0474610

Reference yield:

: 3521-91-3,85520-72-5,111321-98-3,67760-84-3
(4R)-hept-1-en-ol

: 850538-37-3
(2S,6R)-N-(2-nitrobenzenesulfonyl)-6-pent-4-enyl-2-propyl-1,2,3,6-tetrahydropyridine

Guidance literature:: Multi-step reaction with 6 steps

1: 90 percent / Et₃N / CH₂Cl₂ / 3 h / 20 °C

2: 97 percent / NaN₃ / dimethylsulfoxide / 20 h / 50 °C

3: LiAlH₄ / diethyl ether / 3 h / 20 °C

4: 89 percent / K₂CO₃ / CH₂Cl₂ / 24 h / 20 °C

5: 83 percent / PPh₃; DIAD / tetrahydrofuran / 72 h / 20 °C

6: 96 percent / ethylene / Grubbs I catalyst / CH₂Cl₂ / 24 h / 50 °C

With lithium aluminium tetrahydride; sodium azide; ethene; di-isopropyl azodicarboxylate; potassium carbonate; triethylamine; triphenylphosphine; Grubbs catalyst first generation; In tetrahydrofuran; diethyl ether; dichloromethane; dimethyl sulfoxide; 5: Mitsunobu reaction;
DOI:10.1021/ol0474610