2-{3-[(1R,2R)-2-carboxy-1-(2-chloro-benzyl)-2-hydroxy-ethylcarbamoyl]-propyl}-benzoic acid

Base Information

Chemical Name:2-{3-[(1R,2R)-2-carboxy-1-(2-chloro-benzyl)-2-hydroxy-ethylcarbamoyl]-propyl}-benzoic acid
CAS No.:1415481-69-4
Molecular Formula:C₂₁H₂₂ClNO₆
Molecular Weight:419.862
Hs Code.:

Synonyms:2-{3-[(1R,2R)-2-carboxy-1-(2-chloro-benzyl)-2-hydroxy-ethylcarbamoyl]-propyl}-benzoic acid

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Chemical Property of 2-{3-[(1R,2R)-2-carboxy-1-(2-chloro-benzyl)-2-hydroxy-ethylcarbamoyl]-propyl}-benzoic acid

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Technology Process of 2-{3-[(1R,2R)-2-carboxy-1-(2-chloro-benzyl)-2-hydroxy-ethylcarbamoyl]-propyl}-benzoic acid

There total 8 articles about 2-{3-[(1R,2R)-2-carboxy-1-(2-chloro-benzyl)-2-hydroxy-ethylcarbamoyl]-propyl}-benzoic 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:

: 1415481-70-7
2-{3-[(1R,2R)-2-butoxycarbonyl-1-(2-chloro-benzyl)-2-hydroxy-ethylcarbamoyl]-propyl}-benzoic acid

: 1415481-69-4
2-{3-[(1R,2R)-2-carboxy-1-(2-chloro-benzyl)-2-hydroxy-ethylcarbamoyl]-propyl}-benzoic acid

Guidance literature:: 2-{3-[(1R,2R)-2-butoxycarbonyl-1-(2-chloro-benzyl)-2-hydroxy-ethylcarbamoyl]-propyl}-benzoic acid; With water; sodium hydroxide; In tetrahydrofuran; at 20 ℃; for 1h;

With acetic acid; In tetrahydrofuran;

Reference yield:

: 80126-50-7
(R)-2'-chlorophenylalanine

: 1415481-69-4
2-{3-[(1R,2R)-2-carboxy-1-(2-chloro-benzyl)-2-hydroxy-ethylcarbamoyl]-propyl}-benzoic acid

Guidance literature:: Multi-step reaction with 8 steps

1.1: sodium hydroxide; water / 0 °C

1.2: 4 h / pH 8 - 9

1.3: pH 1

2.1: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / dichloromethane / 20 °C

3.1: lithium aluminium tetrahydride / tetrahydrofuran / -20 °C

4.1: sodium hydrogensulfite / water; tetrahydrofuran / 0 °C

5.1: hydrogenchloride / 1,4-dioxane / Reflux

5.2: 4 h / Reflux

6.1: hydrogenchloride / 24 h / 70 °C

7.1: N-ethyl-N,N-diisopropylamine; HATU / dichloromethane / 0.17 h

7.2: 1 h

8.1: sodium hydroxide; water / tetrahydrofuran / 1 h / 20 °C

With hydrogenchloride; lithium aluminium tetrahydride; water; benzotriazol-1-ol; sodium hydrogensulfite; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; HATU; sodium hydroxide; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water;

Reference yield:

: 1415312-30-9
(2R,3R)-3-Amino-4-(2-chloro-phenyl)-2-hydroxy-butyric acid ethyl ester

: 1415481-69-4
2-{3-[(1R,2R)-2-carboxy-1-(2-chloro-benzyl)-2-hydroxy-ethylcarbamoyl]-propyl}-benzoic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: hydrogenchloride / 24 h / 70 °C

2.1: N-ethyl-N,N-diisopropylamine; HATU / dichloromethane / 0.17 h

2.2: 1 h

3.1: sodium hydroxide; water / tetrahydrofuran / 1 h / 20 °C

With hydrogenchloride; water; N-ethyl-N,N-diisopropylamine; HATU; sodium hydroxide; In tetrahydrofuran; dichloromethane;