(4S,5S)-3-(tert-butoxycarbonyl)-4-(cyclohexylmethyl)-2,2-dimethyl-5-<2-(2-pyridylthio)ethyl>oxazolidine

Base Information

Chemical Name:(4S,5S)-3-(tert-butoxycarbonyl)-4-(cyclohexylmethyl)-2,2-dimethyl-5-<2-(2-pyridylthio)ethyl>oxazolidine
CAS No.:143122-20-7
Molecular Formula:C₂₄H₃₈N₂O₃S
Molecular Weight:434.643
Hs Code.:

Synonyms:(4S,5S)-3-(tert-butoxycarbonyl)-4-(cyclohexylmethyl)-2,2-dimethyl-5-<2-(2-pyridylthio)ethyl>oxazolidine

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Chemical Property of (4S,5S)-3-(tert-butoxycarbonyl)-4-(cyclohexylmethyl)-2,2-dimethyl-5-<2-(2-pyridylthio)ethyl>oxazolidine

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Technology Process of (4S,5S)-3-(tert-butoxycarbonyl)-4-(cyclohexylmethyl)-2,2-dimethyl-5-<2-(2-pyridylthio)ethyl>oxazolidine

There total 4 articles about (4S,5S)-3-(tert-butoxycarbonyl)-4-(cyclohexylmethyl)-2,2-dimethyl-5-<2-(2-pyridylthio)ethyl>oxazolidine 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:

: 124577-55-5
(4S,5S)-3-(tert-butoxycarbonyl)-4-(cyclohexylmethyl)-2,2-dimethyloxazolidine-5-ethanol

: 143122-20-7
(4S,5S)-3-(tert-butoxycarbonyl)-4-(cyclohexylmethyl)-2,2-dimethyl-5-<2-(2-pyridylthio)ethyl>oxazolidine

Guidance literature:: Multi-step reaction with 2 steps

1: 86 percent / triethylamine / CH₂Cl₂ / 6 h / Ambient temperature

2: 1.) sodium hydride / 1.) DMF, RT, 30 min, 2.) DMF, RT, 14 h

With sodium hydride; triethylamine; In dichloromethane;
DOI:10.1021/jm00097a010

Reference yield:

: 143122-11-6
(4S,5S)-5-allyl-3-(tert-butoxycarbonyl)-4-(cyclohexylmethyl)-2,2-dimethyloxazolidine

: 143122-20-7
(4S,5S)-3-(tert-butoxycarbonyl)-4-(cyclohexylmethyl)-2,2-dimethyl-5-<2-(2-pyridylthio)ethyl>oxazolidine

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) ozone, 2.) Me₂S / 1.) GH₂Cl₂, -78 deg C, 2.) CH₂Cl₂, RT, overnight

2: sodium borohydride / methanol / 3 h / 0 °C

3: 86 percent / triethylamine / CH₂Cl₂ / 6 h / Ambient temperature

4: 1.) sodium hydride / 1.) DMF, RT, 30 min, 2.) DMF, RT, 14 h

With sodium tetrahydroborate; dimethylsulfide; sodium hydride; ozone; triethylamine; In methanol; dichloromethane;
DOI:10.1021/jm00097a010

Reference yield:

: 145341-80-6
(4S,5S)-3-(tert-butoxycarbonyl)-4-cyclohexylmethyl-5-formylmethyl-2,2-dimethyl-1,3-oxazolidine

: 143122-20-7
(4S,5S)-3-(tert-butoxycarbonyl)-4-(cyclohexylmethyl)-2,2-dimethyl-5-<2-(2-pyridylthio)ethyl>oxazolidine

Guidance literature:: Multi-step reaction with 3 steps

1: sodium borohydride / methanol / 3 h / 0 °C

2: 86 percent / triethylamine / CH₂Cl₂ / 6 h / Ambient temperature

3: 1.) sodium hydride / 1.) DMF, RT, 30 min, 2.) DMF, RT, 14 h

With sodium tetrahydroborate; sodium hydride; triethylamine; In methanol; dichloromethane;
DOI:10.1021/jm00097a010