(S)-2-(3-Chloro-propyl)-4-oxo-3,4-dihydro-2H-pyridine-1-carboxylic acid benzyl ester

Base Information

Chemical Name:(S)-2-(3-Chloro-propyl)-4-oxo-3,4-dihydro-2H-pyridine-1-carboxylic acid benzyl ester
CAS No.:197841-62-6
Molecular Formula:C₁₆H₁₈ClNO₃
Molecular Weight:307.777
Hs Code.:

Synonyms:(S)-2-(3-Chloro-propyl)-4-oxo-3,4-dihydro-2H-pyridine-1-carboxylic acid benzyl ester

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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)-2-(3-Chloro-propyl)-4-oxo-3,4-dihydro-2H-pyridine-1-carboxylic acid benzyl ester

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Technology Process of (S)-2-(3-Chloro-propyl)-4-oxo-3,4-dihydro-2H-pyridine-1-carboxylic acid benzyl ester

There total 5 articles about (S)-2-(3-Chloro-propyl)-4-oxo-3,4-dihydro-2H-pyridine-1-carboxylic acid benzyl ester 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: 94.0%

: 197841-61-5
(S)-2-(3-Hydroxy-propyl)-4-oxo-3,4-dihydro-2H-pyridine-1-carboxylic acid benzyl ester

: 197841-62-6
(S)-2-(3-Chloro-propyl)-4-oxo-3,4-dihydro-2H-pyridine-1-carboxylic acid benzyl ester

Guidance literature:: With N-chloro-succinimide; triphenylphosphine; In dichloromethane; 1.) -42 deg C, 30 min, 2.) room temperature, 4 h;
DOI:10.1021/jo971448u

Reference yield:

: 126378-42-5
4-methoxy-3-(trisopropylsilyl)pyridine

: 197841-62-6
(S)-2-(3-Chloro-propyl)-4-oxo-3,4-dihydro-2H-pyridine-1-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: toluene / 1.5 h / -42 °C

2: 2.) oxalic acid / 1.) THF, -78 deg C, 4 h, 2.) H₂O, room temperature, overnight

3: 1.) NaIO₄, OsO₄, 2.) L-Selectride, 3.) NaBO₃*4H₂O / 1.) H₂O, THF, room temperature, 19 h, 2.) THF, -78 deg C, 1 h, 3.) -78 deg C to room temperature, 3 h

4: 1.) NaOMe, 2.) 10percent HCl / 1.) MeOH, reflux, 3.5 h, 2.) room temperature, 15 min

5: 79 percent / n-BuLi / tetrahydrofuran; hexane / 2 h / -78 °C

6: 94 percent / PPh₃, NCS / CH₂Cl₂ / 1.) -42 deg C, 30 min, 2.) room temperature, 4 h

With hydrogenchloride; sodium perborate; sodium periodate; N-chloro-succinimide; osmium(VIII) oxide; n-butyllithium; sodium methylate; oxalic acid; L-Selectride; triphenylphosphine; In tetrahydrofuran; hexane; dichloromethane; toluene;
DOI:10.1021/jo971448u

Reference yield:

: 501-53-1,94274-21-2
benzyl chloroformate

: 197841-62-6
(S)-2-(3-Chloro-propyl)-4-oxo-3,4-dihydro-2H-pyridine-1-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 79 percent / n-BuLi / tetrahydrofuran; hexane / 2 h / -78 °C

2: 94 percent / PPh₃, NCS / CH₂Cl₂ / 1.) -42 deg C, 30 min, 2.) room temperature, 4 h

With N-chloro-succinimide; n-butyllithium; triphenylphosphine; In tetrahydrofuran; hexane; dichloromethane;
DOI:10.1021/jo971448u