tert-butyl (3S,5S,6R)-3-[(R)-4-amino-3-(trimethylsilyloxy)butyl]-2-oxo-5,6-diphenylmorpholine-4-carboxylate

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Chemical Name:tert-butyl (3S,5S,6R)-3-[(R)-4-amino-3-(trimethylsilyloxy)butyl]-2-oxo-5,6-diphenylmorpholine-4-carboxylate
CAS No.:937183-42-1
Molecular Formula:C₂₈H₄₀N₂O₅Si
Molecular Weight:512.721
Hs Code.:

Synonyms:tert-butyl (3S,5S,6R)-3-[(R)-4-amino-3-(trimethylsilyloxy)butyl]-2-oxo-5,6-diphenylmorpholine-4-carboxylate

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Chemical Property of tert-butyl (3S,5S,6R)-3-[(R)-4-amino-3-(trimethylsilyloxy)butyl]-2-oxo-5,6-diphenylmorpholine-4-carboxylate

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Technology Process of tert-butyl (3S,5S,6R)-3-[(R)-4-amino-3-(trimethylsilyloxy)butyl]-2-oxo-5,6-diphenylmorpholine-4-carboxylate

There total 2 articles about tert-butyl (3S,5S,6R)-3-[(R)-4-amino-3-(trimethylsilyloxy)butyl]-2-oxo-5,6-diphenylmorpholine-4-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: 94.0%

: 937183-41-0
tert-butyl (3S,5S,6R)-3-[(R)-4-azido-3-(trimethylsilyloxy)butyl]-2-oxo-5,6-diphenylmorpholine-4-carboxylate

: 937183-42-1
tert-butyl (3S,5S,6R)-3-[(R)-4-amino-3-(trimethylsilyloxy)butyl]-2-oxo-5,6-diphenylmorpholine-4-carboxylate

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethyl acetate; at 20 ℃; for 20h; atmospheric pressure;
DOI:10.1021/jo070136g

Reference yield:

: 753010-16-1
tert-butyl (3S,5S,6R)-3-[(3R)-4-azido-3-hydroxybutyl]-2-oxo-5,6-diphenyl-1,4-oxazine-4-carboxylate

: 937183-42-1
tert-butyl (3S,5S,6R)-3-[(R)-4-amino-3-(trimethylsilyloxy)butyl]-2-oxo-5,6-diphenylmorpholine-4-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / triethylamine; 4-(N,N-dimethylamino)pyridine / tetrahydrofuran / 7 h / 20 °C

2: 94 percent / hydrogen / Pd/C / ethyl acetate / 20 h / 20 °C / atmospheric pressure

With dmap; hydrogen; triethylamine; palladium on activated charcoal; In tetrahydrofuran; ethyl acetate;
DOI:10.1021/jo070136g