1-(1,3-dihydro-1-hydroxy-2,1-benzoxaborol-6-yl)pyrrole-2-carboxylic acid cyclohexylamide

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Chemical Name:1-(1,3-dihydro-1-hydroxy-2,1-benzoxaborol-6-yl)pyrrole-2-carboxylic acid cyclohexylamide
CAS No.:1615684-96-2
Molecular Formula:C₁₈H₂₁BN₂O₃
Molecular Weight:324.187
Hs Code.:

Synonyms:1-(1,3-dihydro-1-hydroxy-2,1-benzoxaborol-6-yl)pyrrole-2-carboxylic acid cyclohexylamide

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Chemical Property of 1-(1,3-dihydro-1-hydroxy-2,1-benzoxaborol-6-yl)pyrrole-2-carboxylic acid cyclohexylamide

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Technology Process of 1-(1,3-dihydro-1-hydroxy-2,1-benzoxaborol-6-yl)pyrrole-2-carboxylic acid cyclohexylamide

There total 11 articles about 1-(1,3-dihydro-1-hydroxy-2,1-benzoxaborol-6-yl)pyrrole-2-carboxylic acid cyclohexylamide 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: 50.4%

: 1615684-94-0
1-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)-1H-pyrrole-2-carboxylic acid

: 108-91-8,157973-60-9
cyclohexylamine

: 1615684-96-2
1-(1,3-dihydro-1-hydroxy-2,1-benzoxaborol-6-yl)pyrrole-2-carboxylic acid cyclohexylamide

Guidance literature:: 1-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)-1H-pyrrole-2-carboxylic acid; With benzotriazol-1-ol; 1,2-dichloro-ethane; In dichloromethane; at 0 - 20 ℃; for 0.5h;

cyclohexylamine; In dichloromethane;
DOI:10.1016/j.ejmech.2014.04.079

Reference yield:

: 856794-72-4
2-bromo-4-nitrobenzoyl chloride

: 1615684-96-2
1-(1,3-dihydro-1-hydroxy-2,1-benzoxaborol-6-yl)pyrrole-2-carboxylic acid cyclohexylamide

Guidance literature:: Multi-step reaction with 9 steps

1.1: triethylamine / 1 h / 0 - 20 °C

2.1: tin(II) chloride dihdyrate / ethyl acetate / 4 h / Reflux

3.1: ethyl acetate / 4 h / Reflux

4.1: lithium borohydride / tetrahydrofuran / 0 - 20 °C / Inert atmosphere

5.1: n-butyllithium / tetrahydrofuran / 0.25 h / -78 °C / Inert atmosphere

5.2: 20 °C / Inert atmosphere

6.1: hydrogenchloride / water; tetrahydrofuran / Inert atmosphere

7.1: trichlorophosphate / 0.25 h / 0 - 20 °C / Inert atmosphere

7.2: 1.25 h / 0 °C / Inert atmosphere

8.1: silver nitrate; sodium hydroxide / water / 0 - 20 °C / Inert atmosphere

9.1: 1,2-dichloro-ethane; benzotriazol-1-ol / dichloromethane / 0.5 h / 0 - 20 °C

With hydrogenchloride; lithium borohydride; n-butyllithium; tin(II) chloride dihdyrate; benzotriazol-1-ol; silver nitrate; 1,2-dichloro-ethane; triethylamine; sodium hydroxide; trichlorophosphate; In tetrahydrofuran; dichloromethane; water; ethyl acetate;
DOI:10.1016/j.ejmech.2014.04.079

Reference yield:

: C₁₇H₂₄BNO₃

: 1615684-96-2
1-(1,3-dihydro-1-hydroxy-2,1-benzoxaborol-6-yl)pyrrole-2-carboxylic acid cyclohexylamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: hydrogenchloride / water; tetrahydrofuran / Inert atmosphere

2.1: trichlorophosphate / 0.25 h / 0 - 20 °C / Inert atmosphere

2.2: 1.25 h / 0 °C / Inert atmosphere

3.1: silver nitrate; sodium hydroxide / water / 0 - 20 °C / Inert atmosphere

4.1: 1,2-dichloro-ethane; benzotriazol-1-ol / dichloromethane / 0.5 h / 0 - 20 °C

With hydrogenchloride; benzotriazol-1-ol; silver nitrate; 1,2-dichloro-ethane; sodium hydroxide; trichlorophosphate; In tetrahydrofuran; dichloromethane; water;
DOI:10.1016/j.ejmech.2014.04.079