(5R,7R,8S,10R,11R,11aS)-5-benzoyloxymethyl-7-cyano-10-hydroxymethyl-4-methoxy-13-methyl-5,7,8,9,10,11,11a,12-octahydro-8,11-iminoazepino<1,2-b>isoquinoline

Base Information

• Chemical Name: (5R,7R,8S,10R,11R,11aS)-5-benzoyloxymethyl-7-cyano-10-hydroxymethyl-4-methoxy-13-methyl-5,7,8,9,10,11,11a,12-octahydro-8,11-iminoazepino<1,2-b>isoquinoline
• CAS No.: 156246-79-6
• Molecular Formula: C₂₆H₂₉N₃O₄
• Molecular Weight: 447.534
• Mol file: 156246-79-6.mol

Synonyms:(5R,7R,8S,10R,11R,11aS)-5-benzoyloxymethyl-7-cyano-10-hydroxymethyl-4-methoxy-13-methyl-5,7,8,9,10,11,11a,12-octahydro-8,11-iminoazepino<1,2-b>isoquinoline

Chemical Property of (5R,7R,8S,10R,11R,11aS)-5-benzoyloxymethyl-7-cyano-10-hydroxymethyl-4-methoxy-13-methyl-5,7,8,9,10,11,11a,12-octahydro-8,11-iminoazepino<1,2-b>isoquinoline

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (5R,7R,8S,10R,11R,11aS)-5-benzoyloxymethyl-7-cyano-10-hydroxymethyl-4-methoxy-13-methyl-5,7,8,9,10,11,11a,12-octahydro-8,11-iminoazepino<1,2-b>isoquinoline

There total 4 articles about (5R,7R,8S,10R,11R,11aS)-5-benzoyloxymethyl-7-cyano-10-hydroxymethyl-4-methoxy-13-methyl-5,7,8,9,10,11,11a,12-octahydro-8,11-iminoazepino<1,2-b>isoquinoline 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:

C30H33N3O7 (156246-78-5) → (5R,7R,8S,10R,11R,11aS)-5-benzoyloxymethyl-7-cyano-10-hydroxymethyl-4-methoxy-13-methyl-5,7,8,9,10,11,11a,12-octahydro-8,11-iminoazepino<1,2-b>isoquinoline (156246-79-6)

Guidance literature:

With sodium tetrahydroborate; In tetrahydrofuran; for 1h; Yield given; Ambient temperature;

DOI:10.1016/S0040-4020(01)80645-1

Reference yield:

benzoyl chloride (98-88-4) → (5R,7R,8S,10R,11R,11aS)-5-benzoyloxymethyl-7-cyano-10-hydroxymethyl-4-methoxy-13-methyl-5,7,8,9,10,11,11a,12-octahydro-8,11-iminoazepino<1,2-b>isoquinoline (156246-79-6)

Guidance literature:

Multi-step reaction with 3 steps

1: 33 percent / pyridine / 2 h / 0 °C

2: triethylamine / tetrahydrofuran / 2 h

3: sodium borohydride / tetrahydrofuran / 1 h / Ambient temperature

With pyridine; sodium tetrahydroborate; triethylamine; In tetrahydrofuran;

DOI:10.1016/S0040-4020(01)80645-1

Reference yield:

<5R-(5α,7β,8β,10β,11β,11aβ)>-7-cyano-5,7,8,9,10,11,11a,12-octahydro-4-methoxy-5-(hydroxymethyl)-13-methyl-8,11-iminoazepino<1,2-b>isoquinoline-10-carboxylic acid (96251-59-1) → (5R,7R,8S,10R,11R,11aS)-5-benzoyloxymethyl-7-cyano-10-hydroxymethyl-4-methoxy-13-methyl-5,7,8,9,10,11,11a,12-octahydro-8,11-iminoazepino<1,2-b>isoquinoline (156246-79-6)

Guidance literature:

Multi-step reaction with 3 steps

1: 33 percent / pyridine / 2 h / 0 °C

2: triethylamine / tetrahydrofuran / 2 h

3: sodium borohydride / tetrahydrofuran / 1 h / Ambient temperature

With pyridine; sodium tetrahydroborate; triethylamine; In tetrahydrofuran;

DOI:10.1016/S0040-4020(01)80645-1

upstream raw materials:

C₃₀H₃₃N₃O₇

benzoyl chloride

<5R-(5α,7β,8β,10β,11β,11aβ)>-7-cyano-5,7,8,9,10,11,11a,12-octahydro-4-methoxy-5-(hydroxymethyl)-13-methyl-8,11-iminoazepino<1,2-b>isoquinoline-10-carboxylic acid

(5R,7R,8S,10R,11R,11aS)-5-benzoyloxymethyl-7-cyano-4-methoxy-13-methyl-5,7,8,9,10,11,11a,12-octahydro-8,11-iminoazepino<1,2-b>isoquinoline-10-carboxylic acid