C₂₉H₃₅BN₄O₅

Base Information

Chemical Name:C₂₉H₃₅BN₄O₅
CAS No.:1613056-69-1
Molecular Formula:C₂₉H₃₅BN₄O₅
Molecular Weight:530.432
Hs Code.:

C<sub>29</sub>H<sub>35</sub>BN<sub>4</sub>O<sub>5</sub>

Synonyms:C₂₉H₃₅BN₄O₅

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Chemical Property of C₂₉H₃₅BN₄O₅

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Technology Process of C₂₉H₃₅BN₄O₅

There total 5 articles about C₂₉H₃₅BN₄O₅ 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: 70.0%

: 1613056-68-0
methyl ((S)-2-((S)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)pyrrolidin-1-yl)-2-oxo-1-phenylethyl)carbamate

: 73183-34-3
bis(pinacol)diborane

: 1613056-69-1
C₂₉H₃₅BN₄O₅

Guidance literature:: With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium acetate; In N,N-dimethyl-formamide; at 90 ℃; for 3h; Inert atmosphere; Sealed tube;

Reference yield:

: 15761-39-4,59433-50-0
1-(tert-butoxycarbonyl)-L-proline

: 1613056-69-1
C₂₉H₃₅BN₄O₅

Guidance literature:: Multi-step reaction with 5 steps

1: N-ethyl-N,N-diisopropylamine / dichloromethane / 3 h / 0 - 20 °C / Inert atmosphere; Sealed tube

2: ammonium acetate / toluene / 5 h / 110 °C / Inert atmosphere; Sealed tube

3: hydrogenchloride / ethyl acetate / 8 h / 20 °C / Inert atmosphere; Sealed tube

4: N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 3 h / 0 - 20 °C / Inert atmosphere; Sealed tube

5: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium acetate / N,N-dimethyl-formamide / 3 h / 90 °C / Inert atmosphere; Sealed tube

With hydrogenchloride; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; ammonium acetate; potassium acetate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; ethyl acetate; N,N-dimethyl-formamide; toluene;

Reference yield:

: 128120-93-4
(S)-pyrrolidine-1,2-dicarboxylic acid 2-[2-(4-bromophenyl)-2-oxoethyl]ester 1-tert-butyl ester

: 1613056-69-1
C₂₉H₃₅BN₄O₅

Guidance literature:: Multi-step reaction with 4 steps

1: ammonium acetate / toluene / 5 h / 110 °C / Inert atmosphere; Sealed tube

2: hydrogenchloride / ethyl acetate / 8 h / 20 °C / Inert atmosphere; Sealed tube

3: N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 3 h / 0 - 20 °C / Inert atmosphere; Sealed tube

4: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium acetate / N,N-dimethyl-formamide / 3 h / 90 °C / Inert atmosphere; Sealed tube

With hydrogenchloride; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; ammonium acetate; potassium acetate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; ethyl acetate; N,N-dimethyl-formamide; toluene;