(S)-benzyl-1-((1S,2S)-2-benzamido-4-hydroxy-1-phenylbutyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

Base Information

Chemical Name:(S)-benzyl-1-((1S,2S)-2-benzamido-4-hydroxy-1-phenylbutyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate
CAS No.:1621598-86-4
Molecular Formula:C₃₄H₃₄N₂O₄
Molecular Weight:534.655
Hs Code.:

Synonyms:(S)-benzyl-1-((1S,2S)-2-benzamido-4-hydroxy-1-phenylbutyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

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Chemical Property of (S)-benzyl-1-((1S,2S)-2-benzamido-4-hydroxy-1-phenylbutyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

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Technology Process of (S)-benzyl-1-((1S,2S)-2-benzamido-4-hydroxy-1-phenylbutyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

There total 5 articles about (S)-benzyl-1-((1S,2S)-2-benzamido-4-hydroxy-1-phenylbutyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate 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: 95.0%

: 1621598-85-3
N-((1S,2S)-4-hydroxy-1-phenyl-1-((S)-1,2,3,4-tetrahydroisoquinolin-1-yl)butan-2-yl)benzamide

: 501-53-1,94274-21-2
benzyl chloroformate

: 1621598-86-4
(S)-benzyl-1-((1S,2S)-2-benzamido-4-hydroxy-1-phenylbutyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 1h; enantioselective reaction;
DOI:10.1002/chem.201402089

Reference yield:

: 1621598-63-7
((1S,2S,10bS)-2-(2-hydroxyethyl)-1-phenyl-1,2,5,6-tetrahydropyrazolo[5,1-a]isoquinolin-3(10bH)-yl)(phenyl)methanone

: 1621598-86-4
(S)-benzyl-1-((1S,2S)-2-benzamido-4-hydroxy-1-phenylbutyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: samarium diiodide / methanol; tetrahydrofuran / 0.5 h / 20 °C

2: triethylamine / dichloromethane / 1 h / 20 °C

With samarium diiodide; triethylamine; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1002/chem.201402089

Reference yield:

: 1632445-80-7
C₂₆H₂₄N₂O₂

: 1621598-86-4
(S)-benzyl-1-((1S,2S)-2-benzamido-4-hydroxy-1-phenylbutyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: sodium tetrahydroborate / methanol / 2 h / 20 °C

2: samarium diiodide / methanol; tetrahydrofuran / 0.5 h / 20 °C

3: triethylamine / dichloromethane / 1 h / 20 °C

With sodium tetrahydroborate; samarium diiodide; triethylamine; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1002/chem.201402089