(1R,3R)-1-(3,4-dimethoxyphenyl)-3-((R)-1-phenylethylamino)butane-1,4-diol

Base Information

• Chemical Name: (1R,3R)-1-(3,4-dimethoxyphenyl)-3-((R)-1-phenylethylamino)butane-1,4-diol
• CAS No.: 1273328-93-0
• Molecular Formula: C₂₀H₂₇NO₄
• Molecular Weight: 345.439
• Mol file: 1273328-93-0.mol

Synonyms:(1R,3R)-1-(3,4-dimethoxyphenyl)-3-((R)-1-phenylethylamino)butane-1,4-diol

Chemical Property of (1R,3R)-1-(3,4-dimethoxyphenyl)-3-((R)-1-phenylethylamino)butane-1,4-diol

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (1R,3R)-1-(3,4-dimethoxyphenyl)-3-((R)-1-phenylethylamino)butane-1,4-diol

There total 4 articles about (1R,3R)-1-(3,4-dimethoxyphenyl)-3-((R)-1-phenylethylamino)butane-1,4-diol 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: 73.0%

(3R,5R)-5-(3'',4''-dimethoxyphenyl)-3-((R)-1-phenylethylamino)-dihydrofuran-2(3H)-one (1273328-77-0) → (1R,3R)-1-(3,4-dimethoxyphenyl)-3-((R)-1-phenylethylamino)butane-1,4-diol (1273328-93-0)

Guidance literature:

With sodium tetrahydroborate; In ethanol; at 20 ℃;

DOI:10.1021/ol2001057

Reference yield:

(2R)-4-(3,4-dimethoxyphenyl)-4-oxo-2-{[(1R)-1-phenylethyl]amino}butanoic acid (1220353-57-0) → (1R,3R)-1-(3,4-dimethoxyphenyl)-3-((R)-1-phenylethylamino)butane-1,4-diol (1273328-93-0)

Guidance literature:

Multi-step reaction with 4 steps

1: sodium tetrahydroborate / methanol / 20 °C

2: hydrogenchloride / water / 40 °C

3: potassium carbonate / water

4: sodium tetrahydroborate / ethanol / 20 °C

With hydrogenchloride; sodium tetrahydroborate; potassium carbonate; In methanol; ethanol; water;

DOI:10.1021/ol2001057

Reference yield:

C20H25NO5 (1273328-68-9) → (1R,3R)-1-(3,4-dimethoxyphenyl)-3-((R)-1-phenylethylamino)butane-1,4-diol (1273328-93-0)

Guidance literature:

Multi-step reaction with 3 steps

1: hydrogenchloride / water / 40 °C

2: potassium carbonate / water

3: sodium tetrahydroborate / ethanol / 20 °C

With hydrogenchloride; sodium tetrahydroborate; potassium carbonate; In ethanol; water;

DOI:10.1021/ol2001057

upstream raw materials:

(2R)-4-(3,4-dimethoxyphenyl)-4-oxo-2-{[(1R)-1-phenylethyl]amino}butanoic acid

(3R,5R)-5-(3'',4''-dimethoxyphenyl)-3-((R)-1-phenylethylamino)-dihydrofuran-2(3H)-one

C₂₀H₂₅NO₅

(3R,5R)-5-(3'',4''-dimethoxyphenyl)-3-((R)-1-phenylethylamino)-dihydrofuran-2(3H)-one hydrochloride

Downstream raw materials:

(1R,3R)-3-amino-1-(3,4-dimethoxyphenyl)butane-1,4-diol