(1R)-2-endo-[(2S,3R)-3-(Boc-amino)-2-hydroxymethylhydrocinnamoyl]-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol

Base Information

Chemical Name:(1R)-2-endo-[(2S,3R)-3-(Boc-amino)-2-hydroxymethylhydrocinnamoyl]-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol
CAS No.:939959-60-1
Molecular Formula:C₂₅H₃₇NO₅
Molecular Weight:431.572
Hs Code.:

Synonyms:(1R)-2-endo-[(2S,3R)-3-(Boc-amino)-2-hydroxymethylhydrocinnamoyl]-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol

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Chemical Property of (1R)-2-endo-[(2S,3R)-3-(Boc-amino)-2-hydroxymethylhydrocinnamoyl]-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol

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Technology Process of (1R)-2-endo-[(2S,3R)-3-(Boc-amino)-2-hydroxymethylhydrocinnamoyl]-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol

There total 4 articles about (1R)-2-endo-[(2S,3R)-3-(Boc-amino)-2-hydroxymethylhydrocinnamoyl]-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol 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: 96.0%

: 870724-91-7
(3R,4S)-2-benzyl-4-[(1R)-2-exo-hydroxy-1,7,7-trimethylbicyclo[2.2.1]hept-2-ylcarbonyl]-3-phenylisoxazolidine

: 24424-99-5
di-tert-butyl dicarbonate

: 939959-60-1
(1R)-2-endo-[(2S,3R)-3-(Boc-amino)-2-hydroxymethylhydrocinnamoyl]-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; under 1 Torr;
DOI:10.1002/anie.200502308

Reference yield:

: 464-49-3,68546-28-1
(1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one

: 939959-60-1
(1R)-2-endo-[(2S,3R)-3-(Boc-amino)-2-hydroxymethylhydrocinnamoyl]-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol

Guidance literature:: Multi-step reaction with 4 steps

1.1: nBuLi; TMDA / tetrahydrofuran; hexane / 0.5 h / -30 °C

1.2: 75 percent / tetrahydrofuran; hexane / 2 h / -30 °C

2.1: 3.12 g / HCl / H₂O; CH₂Cl₂

3.1: Mg(OTf)2 / CH₂Cl₂ / 72 h / 20 °C

4.1: 96 percent / H₂ / Pd/C / methanol / 1 Torr

With hydrogenchloride; n-butyllithium; hydrogen; magnesium triflate; palladium on activated charcoal; In tetrahydrofuran; methanol; hexane; dichloromethane; water;
DOI:10.1002/anie.200502308

Reference yield:

: 465500-02-1
(1R)-2-endo-propenoyl-1,7,7-trimethylbicyclo[2.2.1]-heptan-2-ol

: 939959-60-1
(1R)-2-endo-[(2S,3R)-3-(Boc-amino)-2-hydroxymethylhydrocinnamoyl]-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol

Guidance literature:: Multi-step reaction with 2 steps

1: Mg(OTf)2 / CH₂Cl₂ / 72 h / 20 °C

2: 96 percent / H₂ / Pd/C / methanol / 1 Torr

With hydrogen; magnesium triflate; palladium on activated charcoal; In methanol; dichloromethane;
DOI:10.1002/anie.200502308