(2S,5R,6R)-6-(benzyloxy)-6-methyl-2-(1'-methylethyl)-1,4-diazabicyclo<3.2.0>heptan-7-one

Base Information

Chemical Name:(2S,5R,6R)-6-(benzyloxy)-6-methyl-2-(1'-methylethyl)-1,4-diazabicyclo<3.2.0>heptan-7-one
CAS No.:141345-46-2
Molecular Formula:C₁₆H₂₂N₂O₂
Molecular Weight:274.363
Hs Code.:

Synonyms:(2S,5R,6R)-6-(benzyloxy)-6-methyl-2-(1'-methylethyl)-1,4-diazabicyclo<3.2.0>heptan-7-one

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Chemical Property of (2S,5R,6R)-6-(benzyloxy)-6-methyl-2-(1'-methylethyl)-1,4-diazabicyclo<3.2.0>heptan-7-one

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Technology Process of (2S,5R,6R)-6-(benzyloxy)-6-methyl-2-(1'-methylethyl)-1,4-diazabicyclo<3.2.0>heptan-7-one

There total 8 articles about (2S,5R,6R)-6-(benzyloxy)-6-methyl-2-(1'-methylethyl)-1,4-diazabicyclo<3.2.0>heptan-7-one 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:

: 141345-40-6
(2S,5R,6R)-4-(benzyloxycarbonyl)-6-(benzyloxy)-6-methyl-2-(1'-methylethyl)-1,4-diazabicyclo<3.2.0>heptan-7-one

: 141345-46-2
(2S,5R,6R)-6-(benzyloxy)-6-methyl-2-(1'-methylethyl)-1,4-diazabicyclo<3.2.0>heptan-7-one

Guidance literature:: With hydrogen; triethylamine; palladium on activated charcoal; In methanol; for 0.0666667h; under 2327.2 Torr;
DOI:10.1021/ja00039a010

Reference yield:

: 2026-48-4,473-75-6
(S)-valinol

: 141345-46-2
(2S,5R,6R)-6-(benzyloxy)-6-methyl-2-(1'-methylethyl)-1,4-diazabicyclo<3.2.0>heptan-7-one

Guidance literature:: Multi-step reaction with 8 steps

1: aq. NaHCO₃ / CH₂Cl₂ / 2 h / Ambient temperature

2: triethylamine / toluene / 0.17 h

3: aq. NaN₃, Bu₄NBr / toluene / 80 - 95 °C

4: 51 percent / H₂ / 10percent Pd/C / methanol / 144 h / 2068.6 Torr

5: silver cyanide / Heating

6: 0.75 g / triethylamine / tetrahydrofuran / 4 h / Ambient temperature

7: 54 percent / acetonitrile / 12 h / Irradiation

8: H₂, triethylamine / 5percent Pd/C / methanol / 0.07 h / 2327.2 Torr

With sodium azide; silver cyanide; tetrabutylammomium bromide; hydrogen; sodium hydrogencarbonate; triethylamine; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; toluene; acetonitrile;
DOI:10.1021/ja00039a010

Reference yield:

: 40630-14-6
(S)-(+)-1,2-diamino-3-methylbutane

: 141345-46-2
(2S,5R,6R)-6-(benzyloxy)-6-methyl-2-(1'-methylethyl)-1,4-diazabicyclo<3.2.0>heptan-7-one

Guidance literature:: Multi-step reaction with 4 steps

1: silver cyanide / Heating

2: 0.75 g / triethylamine / tetrahydrofuran / 4 h / Ambient temperature

3: 54 percent / acetonitrile / 12 h / Irradiation

4: H₂, triethylamine / 5percent Pd/C / methanol / 0.07 h / 2327.2 Torr

With silver cyanide; hydrogen; triethylamine; palladium on activated charcoal; In tetrahydrofuran; methanol; acetonitrile;
DOI:10.1021/ja00039a010