(2R)-N-[(2S)-2-((diphenylmethylidene)amino)-2-(2',6'-difluoro-3',4'-dimethoxybenzyl)-ethan-1-oyl]bornane-10,2-sultam

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Chemical Name:(2R)-N-[(2S)-2-((diphenylmethylidene)amino)-2-(2',6'-difluoro-3',4'-dimethoxybenzyl)-ethan-1-oyl]bornane-10,2-sultam
CAS No.:476359-35-0
Molecular Formula:C₃₄H₃₆F₂N₂O₅S
Molecular Weight:622.733
Hs Code.:

Synonyms:(2R)-N-[(2S)-2-((diphenylmethylidene)amino)-2-(2',6'-difluoro-3',4'-dimethoxybenzyl)-ethan-1-oyl]bornane-10,2-sultam

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Chemical Property of (2R)-N-[(2S)-2-((diphenylmethylidene)amino)-2-(2',6'-difluoro-3',4'-dimethoxybenzyl)-ethan-1-oyl]bornane-10,2-sultam

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Technology Process of (2R)-N-[(2S)-2-((diphenylmethylidene)amino)-2-(2',6'-difluoro-3',4'-dimethoxybenzyl)-ethan-1-oyl]bornane-10,2-sultam

There total 3 articles about (2R)-N-[(2S)-2-((diphenylmethylidene)amino)-2-(2',6'-difluoro-3',4'-dimethoxybenzyl)-ethan-1-oyl]bornane-10,2-sultam 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: 87.0%

: 138566-17-3
2-(benzhydrylideneamino)-1-(10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1.5]dec-4-yl)ethanone

: 476359-31-6
2-chloromethyl-1,3-difluoro-4,5-dimethoxy-benzene

: 476359-35-0
(2R)-N-[(2S)-2-((diphenylmethylidene)amino)-2-(2',6'-difluoro-3',4'-dimethoxybenzyl)-ethan-1-oyl]bornane-10,2-sultam

Guidance literature:: With tetrabutylammomium bromide; potassium carbonate; In acetonitrile; at 50 ℃;
DOI:10.1016/S0957-4166(02)00321-X

Reference yield:

: 71924-61-3
3-fluoro-4,5-dimethoxybenzaldehyde

: 476359-35-0
(2R)-N-[(2S)-2-((diphenylmethylidene)amino)-2-(2',6'-difluoro-3',4'-dimethoxybenzyl)-ethan-1-oyl]bornane-10,2-sultam

Guidance literature:: Multi-step reaction with 3 steps

1: NaBH₄ / tetrahydrofuran / 1 h / 40 °C

2: 617 mg / aq. HCl / 0.5 h / 110 °C

3: 87 percent / K₂CO₃; Bu₄NBr / acetonitrile / 50 °C

With hydrogenchloride; sodium tetrahydroborate; tetrabutylammomium bromide; potassium carbonate; In tetrahydrofuran; acetonitrile;
DOI:10.1016/S0957-4166(02)00321-X

Reference yield:

: 99423-94-6
(3-fluoro-4,5-dimethoxy-phenyl)-methanol

: 476359-35-0
(2R)-N-[(2S)-2-((diphenylmethylidene)amino)-2-(2',6'-difluoro-3',4'-dimethoxybenzyl)-ethan-1-oyl]bornane-10,2-sultam

Guidance literature:: Multi-step reaction with 2 steps

1: 617 mg / aq. HCl / 0.5 h / 110 °C

2: 87 percent / K₂CO₃; Bu₄NBr / acetonitrile / 50 °C

With hydrogenchloride; tetrabutylammomium bromide; potassium carbonate; In acetonitrile;
DOI:10.1016/S0957-4166(02)00321-X