2-((1R,2S,4R,5S)-5-(tert-butyldiphenylsilyloxy)bicyclo[2.2.1]heptan-2-ylamino)-5-isopropyl-5-methylthiazol-4(5H)-one

Base Information

Chemical Name:2-((1R,2S,4R,5S)-5-(tert-butyldiphenylsilyloxy)bicyclo[2.2.1]heptan-2-ylamino)-5-isopropyl-5-methylthiazol-4(5H)-one
CAS No.:1334758-84-7
Molecular Formula:C₃₀H₄₀N₂O₂SSi
Molecular Weight:520.811
Hs Code.:

Synonyms:2-((1R,2S,4R,5S)-5-(tert-butyldiphenylsilyloxy)bicyclo[2.2.1]heptan-2-ylamino)-5-isopropyl-5-methylthiazol-4(5H)-one

Suppliers and Price of 2-((1R,2S,4R,5S)-5-(tert-butyldiphenylsilyloxy)bicyclo[2.2.1]heptan-2-ylamino)-5-isopropyl-5-methylthiazol-4(5H)-one

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 2-((1R,2S,4R,5S)-5-(tert-butyldiphenylsilyloxy)bicyclo[2.2.1]heptan-2-ylamino)-5-isopropyl-5-methylthiazol-4(5H)-one

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-((1R,2S,4R,5S)-5-(tert-butyldiphenylsilyloxy)bicyclo[2.2.1]heptan-2-ylamino)-5-isopropyl-5-methylthiazol-4(5H)-one

There total 10 articles about 2-((1R,2S,4R,5S)-5-(tert-butyldiphenylsilyloxy)bicyclo[2.2.1]heptan-2-ylamino)-5-isopropyl-5-methylthiazol-4(5H)-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: 74.0%

: 1334758-82-5
2-((1R,2S,4R,5S)-5-(tert-butyldiphenylsilyloxy)bicyclo[2.2.1]heptan-2-ylamino)-5-isopropylthiazol-4(5H)-one

: 74-88-4
methyl iodide

: 1334758-84-7
2-((1R,2S,4R,5S)-5-(tert-butyldiphenylsilyloxy)bicyclo[2.2.1]heptan-2-ylamino)-5-isopropyl-5-methylthiazol-4(5H)-one

Guidance literature:: 2-((1R,2S,4R,5S)-5-(tert-butyldiphenylsilyloxy)bicyclo[2.2.1]heptan-2-ylamino)-5-isopropylthiazol-4(5H)-one; With lithium diisopropyl amide; In tetrahydrofuran; hexanes; at -78 ℃; for 1h; Inert atmosphere;

methyl iodide; In tetrahydrofuran; hexanes; at -78 - -40 ℃; for 3h; Inert atmosphere;
DOI:10.1021/ml2001467

Reference yield:

: 1334758-60-9
((1R,2S,4R,5S)-5-(benzyloxy)bicyclo[2.2.1]heptan-2-yloxy)(tert-butyl)diphenylsilane

: 1334758-84-7
2-((1R,2S,4R,5S)-5-(tert-butyldiphenylsilyloxy)bicyclo[2.2.1]heptan-2-ylamino)-5-isopropyl-5-methylthiazol-4(5H)-one

Guidance literature:: Multi-step reaction with 8 steps

1.1: palladium 10% on activated carbon; hydrogen / methanol / 24 h / 20 °C

2.1: pyridinium chlorochromate / dichloromethane / 16 h / 0 °C

3.1: L-Selectride / tetrahydrofuran / 3 h / -78 °C / Inert atmosphere

4.1: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 32 h / 20 °C / Inert atmosphere

5.1: hydrazine / ethanol / 3 h / Reflux; Inert atmosphere

6.1: chloroform / 20 °C / Inert atmosphere

7.1: N-ethyl-N,N-diisopropylamine / ethanol / 1 h / 150 °C / Microwave irradiation

8.1: lithium diisopropyl amide / tetrahydrofuran; hexanes / 1 h / -78 °C / Inert atmosphere

8.2: 3 h / -78 - -40 °C / Inert atmosphere

With palladium 10% on activated carbon; hydrogen; L-Selectride; N-ethyl-N,N-diisopropylamine; triphenylphosphine; pyridinium chlorochromate; hydrazine; lithium diisopropyl amide; diethylazodicarboxylate; In tetrahydrofuran; methanol; hexanes; ethanol; dichloromethane; chloroform; 4.1: Mitsunobu reaction;
DOI:10.1021/ml2001467

Reference yield:

: 1191464-92-2
(1R,2R,4R,5S)-5-(tert-butyldiphenylsilyloxy)bicyclo[2.2.1]heptan-2-ol

: 1334758-84-7
2-((1R,2S,4R,5S)-5-(tert-butyldiphenylsilyloxy)bicyclo[2.2.1]heptan-2-ylamino)-5-isopropyl-5-methylthiazol-4(5H)-one

Guidance literature:: Multi-step reaction with 5 steps

1.1: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 32 h / 20 °C / Inert atmosphere

2.1: hydrazine / ethanol / 3 h / Reflux; Inert atmosphere

3.1: chloroform / 20 °C / Inert atmosphere

4.1: N-ethyl-N,N-diisopropylamine / ethanol / 1 h / 150 °C / Microwave irradiation

5.1: lithium diisopropyl amide / tetrahydrofuran; hexanes / 1 h / -78 °C / Inert atmosphere

5.2: 3 h / -78 - -40 °C / Inert atmosphere

With N-ethyl-N,N-diisopropylamine; triphenylphosphine; hydrazine; lithium diisopropyl amide; diethylazodicarboxylate; In tetrahydrofuran; hexanes; ethanol; chloroform; 1.1: Mitsunobu reaction;
DOI:10.1021/ml2001467