(S)-2-(Diphenyl-phosphinothioyl)-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid ((R)-1-hydroxymethyl-2-methyl-propyl)-amide

Base Information

• Chemical Name: (S)-2-(Diphenyl-phosphinothioyl)-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid ((R)-1-hydroxymethyl-2-methyl-propyl)-amide
• CAS No.: 608533-89-7
• Molecular Formula: C₂₇H₃₁N₂O₂PS
• Molecular Weight: 478.595
• Mol file: 608533-89-7.mol

Synonyms:(S)-2-(Diphenyl-phosphinothioyl)-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid ((R)-1-hydroxymethyl-2-methyl-propyl)-amide

Chemical Property of (S)-2-(Diphenyl-phosphinothioyl)-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid ((R)-1-hydroxymethyl-2-methyl-propyl)-amide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (S)-2-(Diphenyl-phosphinothioyl)-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid ((R)-1-hydroxymethyl-2-methyl-propyl)-amide

There total 5 articles about (S)-2-(Diphenyl-phosphinothioyl)-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid ((R)-1-hydroxymethyl-2-methyl-propyl)-amide 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: 99.0%

(R)-2-amino-3-methylbutanol (4276-09-9,473-75-6) + (S)-2-(Diphenyl-phosphinothioyl)-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid (608533-85-3) → (S)-2-(Diphenyl-phosphinothioyl)-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid ((R)-1-hydroxymethyl-2-methyl-propyl)-amide (608533-89-7)

Guidance literature:

With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; In acetonitrile;

DOI:10.1016/S0040-4039(03)01561-2

Reference yield:

chloro-diphenylphosphine (1079-66-9,74391-44-9) → (S)-2-(Diphenyl-phosphinothioyl)-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid ((R)-1-hydroxymethyl-2-methyl-propyl)-amide (608533-89-7)

Guidance literature:

Multi-step reaction with 4 steps

1: triethylamine / tetrahydrofuran / 12 h / 40 °C

2: sulfur / toluene / 1 h / 20 °C

3: lithium hydroxide / methanol / 24 h / Heating

4: (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine / acetonitrile

With sulfur; lithium hydroxide; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; In tetrahydrofuran; methanol; toluene; acetonitrile;

DOI:10.1016/S0040-4039(03)01561-2

Reference yield:

methyl (3S)-1,2,3,4-tetrahydro-3-isoquinolinecarboxylate (79815-19-3,79799-05-6) → (S)-2-(Diphenyl-phosphinothioyl)-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid ((R)-1-hydroxymethyl-2-methyl-propyl)-amide (608533-89-7)

Guidance literature:

Multi-step reaction with 4 steps

1: triethylamine / tetrahydrofuran / 12 h / 40 °C

2: sulfur / toluene / 1 h / 20 °C

3: lithium hydroxide / methanol / 24 h / Heating

4: (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine / acetonitrile

With sulfur; lithium hydroxide; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; In tetrahydrofuran; methanol; toluene; acetonitrile;

DOI:10.1016/S0040-4039(03)01561-2

upstream raw materials:

(R)-2-amino-3-methylbutanol

(S)-2-(Diphenyl-phosphinothioyl)-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid

chloro-diphenylphosphine

methyl (3S)-1,2,3,4-tetrahydro-3-isoquinolinecarboxylate

Downstream raw materials:

(S)-2-(Diphenyl-phosphinothioyl)-3-((S)-4-isopropyl-4,5-dihydro-oxazol-2-yl)-1,2,3,4-tetrahydro-isoquinoline