[¹⁴C]-(R)-(1-(2-(2,5-dichlorobenzamido)acetamido)-3-methylbutyl)boronic acid

Base Information

Chemical Name:[¹⁴C]-(R)-(1-(2-(2,5-dichlorobenzamido)acetamido)-3-methylbutyl)boronic acid
CAS No.:1529807-54-2
Molecular Formula:C₁₄H₁₉BCl₂N₂O₄
Molecular Weight:363.022
Hs Code.:

[<sup>14</sup>C]-(R)-(1-(2-(2,5-dichlorobenzamido)acetamido)-3-methylbutyl)boronic acid

Synonyms:[¹⁴C]-(R)-(1-(2-(2,5-dichlorobenzamido)acetamido)-3-methylbutyl)boronic acid

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Chemical Property of [¹⁴C]-(R)-(1-(2-(2,5-dichlorobenzamido)acetamido)-3-methylbutyl)boronic acid

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Technology Process of [¹⁴C]-(R)-(1-(2-(2,5-dichlorobenzamido)acetamido)-3-methylbutyl)boronic acid

There total 5 articles about [¹⁴C]-(R)-(1-(2-(2,5-dichlorobenzamido)acetamido)-3-methylbutyl)boronic acid 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: 50.0%

: 1529807-53-1
[¹⁴C]-2,5-dichloro-N-[2-({(1R)-3-methyl-1-[(3aS,4S,6S,7aR)-3a,5,5-trimethylhexahydro-4,6-methano-1,3,2-benzodioaxaborol-2-yl]butyl}amino)-2-oxoethyl]benzamide

: 1529807-54-2
[¹⁴C]-(R)-(1-(2-(2,5-dichlorobenzamido)acetamido)-3-methylbutyl)boronic acid

Guidance literature:: With hydrogenchloride; Dihydroxy-isobutyl-boran; water; In methanol; hexane; at 20 ℃; for 4h; Inert atmosphere;
DOI:10.1002/jlcr.3079

Reference yield:

: 1435-50-3
2-bromo-1,4-dichlorobenzene

: 1529807-54-2
[¹⁴C]-(R)-(1-(2-(2,5-dichlorobenzamido)acetamido)-3-methylbutyl)boronic acid

Guidance literature:: Multi-step reaction with 5 steps

1.1: n-butyllithium / hexane; diethyl ether / 0.5 h / -78 °C / Inert atmosphere

1.2: 4 h / -78 °C / Inert atmosphere

2.1: N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / tetrahydrofuran / 0 - 25 °C / Inert atmosphere

3.1: lithium hydroxide; water / methanol / 20 °C

4.1: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / N,N-dimethyl-formamide / 0.25 h / 20 °C / Inert atmosphere

4.2: 1 h / 0 °C / Inert atmosphere

5.1: Dihydroxy-isobutyl-boran; hydrogenchloride; water / methanol; hexane / 4 h / 20 °C / Inert atmosphere

With hydrogenchloride; n-butyllithium; Dihydroxy-isobutyl-boran; water; benzotriazol-1-ol; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; lithium hydroxide; In tetrahydrofuran; methanol; diethyl ether; hexane; N,N-dimethyl-formamide;
DOI:10.1002/jlcr.3079

Reference yield:

: 1529807-51-9
[¹⁴C]-methyl-[(2,5-dichlorobenzoyl)amino]acetate

: 1529807-54-2
[¹⁴C]-(R)-(1-(2-(2,5-dichlorobenzamido)acetamido)-3-methylbutyl)boronic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: lithium hydroxide; water / methanol / 20 °C

2.1: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / N,N-dimethyl-formamide / 0.25 h / 20 °C / Inert atmosphere

2.2: 1 h / 0 °C / Inert atmosphere

3.1: Dihydroxy-isobutyl-boran; hydrogenchloride; water / methanol; hexane / 4 h / 20 °C / Inert atmosphere

With hydrogenchloride; Dihydroxy-isobutyl-boran; water; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; lithium hydroxide; In methanol; hexane; N,N-dimethyl-formamide;
DOI:10.1002/jlcr.3079