(S)-1-(4-(4-(3-(2-cyclohexylethyl)phenyl)oxazol-2-yl)benzoyl)pyrrolidine-2-carbonitrile

Base Information

Chemical Name:(S)-1-(4-(4-(3-(2-cyclohexylethyl)phenyl)oxazol-2-yl)benzoyl)pyrrolidine-2-carbonitrile
CAS No.:1307310-09-3
Molecular Formula:C₂₉H₃₁N₃O₂
Molecular Weight:453.584
Hs Code.:

Synonyms:(S)-1-(4-(4-(3-(2-cyclohexylethyl)phenyl)oxazol-2-yl)benzoyl)pyrrolidine-2-carbonitrile

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Chemical Property of (S)-1-(4-(4-(3-(2-cyclohexylethyl)phenyl)oxazol-2-yl)benzoyl)pyrrolidine-2-carbonitrile

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Technology Process of (S)-1-(4-(4-(3-(2-cyclohexylethyl)phenyl)oxazol-2-yl)benzoyl)pyrrolidine-2-carbonitrile

There total 13 articles about (S)-1-(4-(4-(3-(2-cyclohexylethyl)phenyl)oxazol-2-yl)benzoyl)pyrrolidine-2-carbonitrile 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: 81.0%

: 1307310-08-2
4-(4-(3-(2-cyclohexylethyl)phenyl)oxazol-2-yl)benzoic acid

: (S)-pyrrolidine-2-carbonitrile trifluoroacetic acid salt

: 1307310-09-3
(S)-1-(4-(4-(3-(2-cyclohexylethyl)phenyl)oxazol-2-yl)benzoyl)pyrrolidine-2-carbonitrile

Guidance literature:: With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 4h; Inert atmosphere;
DOI:10.1021/jm2001053

Reference yield:

: 1307310-02-6
2-bromo-1-(3-(2-cyclohexylethyl)phenyl)ethanone

: 1307310-09-3
(S)-1-(4-(4-(3-(2-cyclohexylethyl)phenyl)oxazol-2-yl)benzoyl)pyrrolidine-2-carbonitrile

Guidance literature:: Multi-step reaction with 3 steps

1.1: caesium carbonate / ethanol / 0.1 h / 20 °C / Sonication; Inert atmosphere

1.2: 12 h / 20 °C / Inert atmosphere

2.1: ammonium acetate; acetic acid / 16 h / Reflux; Inert atmosphere

3.1: benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / dichloromethane / 4 h / 20 °C / Inert atmosphere

With ammonium acetate; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; caesium carbonate; acetic acid; N-ethyl-N,N-diisopropylamine; In ethanol; dichloromethane;
DOI:10.1021/jm2001053

Reference yield:

: 1307310-01-5
1-(3-(2-cyclohexylethyl)phenyl)ethanone

: 1307310-09-3
(S)-1-(4-(4-(3-(2-cyclohexylethyl)phenyl)oxazol-2-yl)benzoyl)pyrrolidine-2-carbonitrile

Guidance literature:: Multi-step reaction with 4 steps

1.1: bromine / chloroform / 40 °C / Inert atmosphere

2.1: caesium carbonate / ethanol / 0.1 h / 20 °C / Sonication; Inert atmosphere

2.2: 12 h / 20 °C / Inert atmosphere

3.1: ammonium acetate; acetic acid / 16 h / Reflux; Inert atmosphere

4.1: benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / dichloromethane / 4 h / 20 °C / Inert atmosphere

With ammonium acetate; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; bromine; caesium carbonate; acetic acid; N-ethyl-N,N-diisopropylamine; In ethanol; dichloromethane; chloroform;
DOI:10.1021/jm2001053