(2R)-2-{(5-chloro-hydroxybenzyl)-3-[(2,4,6-trimethoxybenzyl)amino]propanamide}acetic acid

Base Information

Chemical Name:(2R)-2-{(5-chloro-hydroxybenzyl)-3-[(2,4,6-trimethoxybenzyl)amino]propanamide}acetic acid
CAS No.:1312771-24-6
Molecular Formula:C₂₂H₂₇ClN₂O₇
Molecular Weight:466.919
Hs Code.:

Synonyms:(2R)-2-{(5-chloro-hydroxybenzyl)-3-[(2,4,6-trimethoxybenzyl)amino]propanamide}acetic acid

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Chemical Property of (2R)-2-{(5-chloro-hydroxybenzyl)-3-[(2,4,6-trimethoxybenzyl)amino]propanamide}acetic acid

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Technology Process of (2R)-2-{(5-chloro-hydroxybenzyl)-3-[(2,4,6-trimethoxybenzyl)amino]propanamide}acetic acid

There total 5 articles about (2R)-2-{(5-chloro-hydroxybenzyl)-3-[(2,4,6-trimethoxybenzyl)amino]propanamide}acetic 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:

: 1312771-23-5
ethyl (2R)-2-{(5-chloro-hydroxybenzyl)-3-[(2,4,6-trimethoxybenzyl)amino]propanamide}acetate

: 1312771-24-6
(2R)-2-{(5-chloro-hydroxybenzyl)-3-[(2,4,6-trimethoxybenzyl)amino]propanamide}acetic acid

Guidance literature:: ethyl (2R)-2-{(5-chloro-hydroxybenzyl)-3-[(2,4,6-trimethoxybenzyl)amino]propanamide}acetate; With water; sodium hydroxide; at 20 ℃; for 4h;

With hydrogenchloride; In water;

Reference yield:

: 889857-60-7
(2R)-3-[(tert-butoxycarbonyl)amino]-2-(5-chloro-2-methoxybenzyl)propanoic acid

: 1312771-24-6
(2R)-2-{(5-chloro-hydroxybenzyl)-3-[(2,4,6-trimethoxybenzyl)amino]propanamide}acetic acid

Guidance literature:: Multi-step reaction with 5 steps

1.1: boron tribromide / dichloromethane / 20 °C / Cooling with ice

1.2: Cooling with ice

2.1: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / dichloromethane / 1.5 h / 35 °C

3.1: methanesulfonic acid / ethanol / 6 h / 40 °C

3.2: Cooling with ice

4.1: triethylamine; sodium tris(acetoxy)borohydride / ethanol / 3.5 h / 20 °C / Cooling with ice

4.2: Cooling with ice

5.1: sodium hydroxide; water / 4 h / 20 °C

With methanesulfonic acid; water; boron tribromide; sodium tris(acetoxy)borohydride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; sodium hydroxide; In ethanol; dichloromethane;

Reference yield:

: 1312771-22-4
ethyl (2R)-2-{3-[(tert-butoxycarbonyl)amino]-2-[5-chloro-2-(tert-butoxycarbonyl)oxybenzyl]propanamide}acetate

: 1312771-24-6
(2R)-2-{(5-chloro-hydroxybenzyl)-3-[(2,4,6-trimethoxybenzyl)amino]propanamide}acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: methanesulfonic acid / ethanol / 6 h / 40 °C

1.2: Cooling with ice

2.1: triethylamine; sodium tris(acetoxy)borohydride / ethanol / 3.5 h / 20 °C / Cooling with ice

2.2: Cooling with ice

3.1: sodium hydroxide; water / 4 h / 20 °C

With methanesulfonic acid; water; sodium tris(acetoxy)borohydride; triethylamine; sodium hydroxide; In ethanol;