2-<2-(4,5-diphenyl-2-oxazolyl)ethyl>-1-<(N-Boc-N-allyl)carbamoylmethyl>azetidinone

Base Information

Chemical Name:2-<2-(4,5-diphenyl-2-oxazolyl)ethyl>-1-<(N-Boc-N-allyl)carbamoylmethyl>azetidinone
CAS No.:129374-53-4
Molecular Formula:C₃₀H₃₃N₃O₅
Molecular Weight:515.609
Hs Code.:

Synonyms:2-<2-(4,5-diphenyl-2-oxazolyl)ethyl>-1-<(N-Boc-N-allyl)carbamoylmethyl>azetidinone

Suppliers and Price of 2-<2-(4,5-diphenyl-2-oxazolyl)ethyl>-1-<(N-Boc-N-allyl)carbamoylmethyl>azetidinone

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-<2-(4,5-diphenyl-2-oxazolyl)ethyl>-1-<(N-Boc-N-allyl)carbamoylmethyl>azetidinone

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-<2-(4,5-diphenyl-2-oxazolyl)ethyl>-1-<(N-Boc-N-allyl)carbamoylmethyl>azetidinone

There total 6 articles about 2-<2-(4,5-diphenyl-2-oxazolyl)ethyl>-1-<(N-Boc-N-allyl)carbamoylmethyl>azetidinone 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: 85.0%

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

: 129374-52-3
2-<2-(4,5-diphenyl-2-oxazolyl)ethyl>-1-(N-allylcarbamoylmethyl)azetidinone

: 129374-53-4
2-<2-(4,5-diphenyl-2-oxazolyl)ethyl>-1-<(N-Boc-N-allyl)carbamoylmethyl>azetidinone

Guidance literature:: With dmap; In acetonitrile; at 25 ℃; for 4.5h;

Reference yield:

: 21256-18-8
3-(4,5-Diphenyl-oxazol-2-yl)-propionic acid

: 129374-53-4
2-<2-(4,5-diphenyl-2-oxazolyl)ethyl>-1-<(N-Boc-N-allyl)carbamoylmethyl>azetidinone

Guidance literature:: Multi-step reaction with 6 steps

1: 1.) carbonyldiimidazole / 1.) THF, 25 deg C, 6 h, 2.) 25 deg C

2: 80 percent / ammonium acetate, acetic acid / benzene / 3 h / Heating

3: 87 percent / concd. HCl, NaBH₃CN, Bromokresol Green / tetrahydrofuran; ethanol / 0 °C

4: 87.8 percent / NaOH / methanol / 4 h / Heating

5: 74 percent / H₂O; ethane-1,2-diol; glycerol / 2.5 h / 25 °C

6: 85 percent / DMAP / acetonitrile / 4.5 h / 25 °C

With ammonium acetate; hydrogenchloride; dmap; sodium hydroxide; bromocresol green; sodium cyanoborohydride; acetic acid; 1,1'-carbonyldiimidazole; In tetrahydrofuran; methanol; ethanol; water; ethylene glycol; glycerol; acetonitrile; benzene;

Reference yield:

: 129374-51-2
5-(4,5-diphenyl-2-oxazolyl)-3-aminopentanoic acid

: 129374-53-4
2-<2-(4,5-diphenyl-2-oxazolyl)ethyl>-1-<(N-Boc-N-allyl)carbamoylmethyl>azetidinone

Guidance literature:: Multi-step reaction with 2 steps

1: 74 percent / H₂O; ethane-1,2-diol; glycerol / 2.5 h / 25 °C

2: 85 percent / DMAP / acetonitrile / 4.5 h / 25 °C

With dmap; In water; ethylene glycol; glycerol; acetonitrile;