tert-butyl [(3S)-1-(3-[3-(trifluoromethyl)phenyl]-4,5-dihydroisoxazol-5-ylcarbonyl)pyrrolidin-3-yl]carbamate

Base Information

Chemical Name:tert-butyl [(3S)-1-(3-[3-(trifluoromethyl)phenyl]-4,5-dihydroisoxazol-5-ylcarbonyl)pyrrolidin-3-yl]carbamate
CAS No.:857651-07-1
Molecular Formula:C₂₀H₂₄F₃N₃O₄
Molecular Weight:427.423
Hs Code.:

Synonyms:tert-butyl [(3S)-1-(3-[3-(trifluoromethyl)phenyl]-4,5-dihydroisoxazol-5-ylcarbonyl)pyrrolidin-3-yl]carbamate

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Chemical Property of tert-butyl [(3S)-1-(3-[3-(trifluoromethyl)phenyl]-4,5-dihydroisoxazol-5-ylcarbonyl)pyrrolidin-3-yl]carbamate

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Technology Process of tert-butyl [(3S)-1-(3-[3-(trifluoromethyl)phenyl]-4,5-dihydroisoxazol-5-ylcarbonyl)pyrrolidin-3-yl]carbamate

There total 5 articles about tert-butyl [(3S)-1-(3-[3-(trifluoromethyl)phenyl]-4,5-dihydroisoxazol-5-ylcarbonyl)pyrrolidin-3-yl]carbamate 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:

: 708274-24-2
3-[3-(trifluoromethyl)phenyl]-4,5-dihydroisoxazole-5-carboxylic acid

: 122536-76-9,140629-77-2
3(S)-(tert-butoxycarbonylamino)pyrrolidine

: 857651-07-1
tert-butyl [(3S)-1-(3-[3-(trifluoromethyl)phenyl]-4,5-dihydroisoxazol-5-ylcarbonyl)pyrrolidin-3-yl]carbamate

Guidance literature:: With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; In DMF (N,N-dimethyl-formamide); dichloromethane; at 0 - 20 ℃; for 2h;

Reference yield:

: 454-89-7
3-Trifluoromethylbenzaldehyde

: 857651-07-1
tert-butyl [(3S)-1-(3-[3-(trifluoromethyl)phenyl]-4,5-dihydroisoxazol-5-ylcarbonyl)pyrrolidin-3-yl]carbamate

Guidance literature:: Multi-step reaction with 5 steps

1.1: hydroxylamine hydrochloride; triethylamine / methanol / 3 h / Reflux

2.1: N-chloro-succinimide / dichloromethane / 2 h / 0 - 45 °C

3.1: triethylamine / dichloromethane / 20 h / 0 - 20 °C / Inert atmosphere

4.1: sodium hydroxide; water / tetrahydrofuran / 2 h / 0 - 20 °C

4.2: pH 7

5.1: (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine / dichloromethane; N,N-dimethyl-formamide / 2 h / 0 - 20 °C

With N-chloro-succinimide; hydroxylamine hydrochloride; water; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; sodium hydroxide; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 69053-93-6
α-chloro-(3-trifluoromethylbenzaldehyde)oxime

: 857651-07-1
tert-butyl [(3S)-1-(3-[3-(trifluoromethyl)phenyl]-4,5-dihydroisoxazol-5-ylcarbonyl)pyrrolidin-3-yl]carbamate

Guidance literature:: Multi-step reaction with 3 steps

1.1: triethylamine / dichloromethane / 20 h / 0 - 20 °C / Inert atmosphere

2.1: sodium hydroxide; water / tetrahydrofuran / 2 h / 0 - 20 °C

2.2: pH 7

3.1: (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine / dichloromethane; N,N-dimethyl-formamide / 2 h / 0 - 20 °C

With water; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; sodium hydroxide; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;